The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It carries signals from the retina to the brain. The second order neurons are the retinal ganglion cells whose axons form the optic nerve. The optic chiasm allows fibers from the nasal retina to cross to the opposite side. The optic tracts relay signals from the optic chiasm to the lateral geniculate bodies. The optic radiations then carry signals from the LGBs to the visual cortex in the occipital lobe where visual perception occurs. Lesions in different parts of the visual pathway cause specific visual field defects.
The eye receives its blood supply from two vascular systems - the retinal vessels and the ciliary (uveal) vessels. The retinal vessels include the central retinal artery and vein, which arise from the ophthalmic artery, a branch of the internal carotid artery. The ciliary vessels include the anterior and posterior ciliary arteries. Both systems anastomose to form circulations in the retina and choroid. The choroid has a dense capillary network called the choriocapillaris that supplies the outer retina. The retina and optic nerve have autoregulatory mechanisms to maintain constant blood flow despite changes in perfusion pressure, while the choroid has limited autoregulation.
This document discusses the blood supply of the eye. It begins by outlining the main arteries involved - the ophthalmic artery, cerebral arteries, circle of Willis, and external carotid artery. It then provides detailed descriptions of each artery's origin, course, branches and clinical significance as they relate to supplying structures of the eye. This includes descriptions of the central retinal artery and its branches within the retina, as well as the conjunctival and episcleral arteries. It also briefly discusses the arteries of the brain including the internal and vertebral arteries, basilar artery, and circle of Willis.
This document summarizes various types of gaze palsies, including their causes and clinical presentations. Supranuclear gaze palsies can result from lesions in areas that control eye movements, like the brainstem or cerebral cortex. Clinical exams help localize lesions and differentiate organic from functional disorders. Specific syndromes discussed include Parinaud's syndrome, progressive supranuclear palsy, internuclear ophthalmoplegia, and one-and-a-half syndrome. The document provides details on symptoms, locations of lesions, and distinguishing features of different supranuclear gaze palsy conditions.
1. The pupil is a circular opening located in the center of the iris that regulates the amount of light entering the eye.
2. Pupil size and reaction are controlled by two sets of muscles - the sphincter pupillae constricts the pupil in response to light, and the dilator pupillae dilates the pupil under sympathetic stimulation.
3. Abnormalities in pupil size, shape, reaction to light and near response can indicate underlying pathologies affecting the complex neurological pathways and muscles that control the pupil. Assessment of pupillary reflexes is important for localizing lesions in the afferent visual pathways or efferent autonomic pathways.
The document discusses the anatomy of the orbit, including:
1. The orbit develops from mesenchyme between the 6th and 7th week, with bones forming around the optic vesicle.
2. The bones that make up the orbit include the frontal, ethmoid, sphenoid, lacrimal, palatine, maxillary, and zygomatic bones.
3. The orbit contains the eyeball, orbital fat, connective tissue system, blood vessels, and nerves including the extraocular muscles.
This document provides information on anterior ischemic optic neuropathy (AION), which is the most common cause of acute optic neuropathy in older age groups. It can be divided into two types: arteritic AION, which is due to giant cell arteritis; and non-arteritic AION, which makes up most cases. Both types present with sudden painless vision loss and optic disc swelling. Arteritic AION carries a worse prognosis and requires high-dose steroid treatment to prevent loss of vision in the fellow eye. Non-arteritic AION has a variable course but generally a poor rate of recovery without any proven effective treatments.
The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It carries signals from the retina to the brain. The second order neurons are the retinal ganglion cells whose axons form the optic nerve. The optic chiasm allows fibers from the nasal retina to cross to the opposite side. The optic tracts relay signals from the optic chiasm to the lateral geniculate bodies. The optic radiations then carry signals from the LGBs to the visual cortex in the occipital lobe where visual perception occurs. Lesions in different parts of the visual pathway cause specific visual field defects.
The eye receives its blood supply from two vascular systems - the retinal vessels and the ciliary (uveal) vessels. The retinal vessels include the central retinal artery and vein, which arise from the ophthalmic artery, a branch of the internal carotid artery. The ciliary vessels include the anterior and posterior ciliary arteries. Both systems anastomose to form circulations in the retina and choroid. The choroid has a dense capillary network called the choriocapillaris that supplies the outer retina. The retina and optic nerve have autoregulatory mechanisms to maintain constant blood flow despite changes in perfusion pressure, while the choroid has limited autoregulation.
This document discusses the blood supply of the eye. It begins by outlining the main arteries involved - the ophthalmic artery, cerebral arteries, circle of Willis, and external carotid artery. It then provides detailed descriptions of each artery's origin, course, branches and clinical significance as they relate to supplying structures of the eye. This includes descriptions of the central retinal artery and its branches within the retina, as well as the conjunctival and episcleral arteries. It also briefly discusses the arteries of the brain including the internal and vertebral arteries, basilar artery, and circle of Willis.
This document summarizes various types of gaze palsies, including their causes and clinical presentations. Supranuclear gaze palsies can result from lesions in areas that control eye movements, like the brainstem or cerebral cortex. Clinical exams help localize lesions and differentiate organic from functional disorders. Specific syndromes discussed include Parinaud's syndrome, progressive supranuclear palsy, internuclear ophthalmoplegia, and one-and-a-half syndrome. The document provides details on symptoms, locations of lesions, and distinguishing features of different supranuclear gaze palsy conditions.
1. The pupil is a circular opening located in the center of the iris that regulates the amount of light entering the eye.
2. Pupil size and reaction are controlled by two sets of muscles - the sphincter pupillae constricts the pupil in response to light, and the dilator pupillae dilates the pupil under sympathetic stimulation.
3. Abnormalities in pupil size, shape, reaction to light and near response can indicate underlying pathologies affecting the complex neurological pathways and muscles that control the pupil. Assessment of pupillary reflexes is important for localizing lesions in the afferent visual pathways or efferent autonomic pathways.
The document discusses the anatomy of the orbit, including:
1. The orbit develops from mesenchyme between the 6th and 7th week, with bones forming around the optic vesicle.
2. The bones that make up the orbit include the frontal, ethmoid, sphenoid, lacrimal, palatine, maxillary, and zygomatic bones.
3. The orbit contains the eyeball, orbital fat, connective tissue system, blood vessels, and nerves including the extraocular muscles.
This document provides information on anterior ischemic optic neuropathy (AION), which is the most common cause of acute optic neuropathy in older age groups. It can be divided into two types: arteritic AION, which is due to giant cell arteritis; and non-arteritic AION, which makes up most cases. Both types present with sudden painless vision loss and optic disc swelling. Arteritic AION carries a worse prognosis and requires high-dose steroid treatment to prevent loss of vision in the fellow eye. Non-arteritic AION has a variable course but generally a poor rate of recovery without any proven effective treatments.
Primary optic atrophy occurs due to direct damage to the optic nerve and results in chalky white disc color with well defined margins and normal cupping and vessels. Secondary optic atrophy follows conditions like papilledema that cause swelling first, resulting in a filled cup and dirty white color. Consecutive optic atrophy occurs after other retinal conditions and shows waxy pallor, normal cup and grossly thinned vessels.
The document describes the neural pathway for vision, including the retina, optic nerve, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex. It notes that the pathway involves three orders of neurons. It discusses how the nasal and temporal halves of the retina project to different sides of the brain, causing visual field defects when different areas are damaged. Common lesions that can cause visual field defects include those of the optic nerve, optic chiasm, optic tracts, lateral geniculate nucleus, optic radiations, and occipital lobe.
This document discusses the anatomy and manifestations of lesions along the visual pathway, including the optic nerve, chiasm, optic tract, lateral geniculate bodies, optic radiations, and visual cortex. Key points covered include the structures of each component of the visual pathway and the visual field defects that result from lesions in different locations, such as optic neuropathies, chiasmal syndromes, and homonymous hemianopsias from retrochiasmal lesions. Specific conditions like cortical blindness, dyschromatopsia, alexia without agraphia, and palinopsia that can arise from lesions in different areas are also mentioned.
The document summarizes the blood and nerve supply of the eye and optic nerve. It discusses the arterial supply which comes from branches of the internal and external carotid arteries. It then describes the specific branches like the central retinal artery and posterior ciliary arteries. It provides details on the venous drainage and nerve supply including the trigeminal, oculomotor, trochlear and abducent cranial nerves. In summary, it provides an overview of the arterial blood supply, venous drainage and cranial nerve innervation of the eye and optic nerve.
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anatomy of optic nerve and its blood supply and clinical corelation
Presentation Layout: optic nerve anatomy
Embryology of optic nerve
Introduction
Parts of optic nerve
Blood supply
Clinical significance
For Further Reading
Wolff’s Anatomy of the eye and orbit by Bron, Tripathi and Tripathi
Anatomy and Physiology of eye by A.K. Khurana 2nd edition
Comprehensive Ophthalmology by A.K. Khurana 5th edition
AAO- Fundamentals & Principles of Ophthalmology : sec 2
Walsh and Hoyt’s Clinical Ophthalmology
Internet
The optic nerve has no myelin sheath and is surrounded by meninges. It transmits signals from the retina and has four parts - intraocular, intraorbital, canalicular, and intracranial. The optic nerve head contains zones like the superficial nerve fiber layer, prelaminar zone, lamina cribrosa, and retrolaminar region. The lamina cribrosa provides a blood supply and the nerve increases in diameter after passing through it. In glaucoma, retinal ganglion cell loss leads to cupping of the optic disc. The optic nerve receives blood supply from the ophthalmic and ciliary arteries. Dysfunctions can cause visual field defects, changes to acuity and
The document discusses visual field testing techniques including kinetic methods using moving targets and static methods using stationary targets. It describes common visual field parameters like isopters and various pathologies that can cause visual field defects like glaucoma. Standardized tests are discussed including the tangent screen test and different algorithms used for static threshold tests like SITA. Key aspects of visual field analyzer equipment and reliable interpretation of results are also covered.
The optic nerve develops from the embryonic optic stalk and contains axons originating from retinal ganglion cells. It has intraocular, intraorbital, intracanalicular, and intracranial parts. The intraocular part passes through the lamina cribrosa and expands as it acquires a myelin sheath. The optic nerve receives its blood supply from short posterior ciliary arteries and pial vessels.
The optic nerve receives its blood supply from multiple sources along its path from the eye to the brain. In the eye, it is supplied by retinal arterioles and occasionally the ciliary artery. In the prelaminar region, it receives blood from ciliary region vessels and peripapillary choroidal or short posterior ciliary vessels. Deeper regions receive supply from ciliary and retinal circulations, including recurrent pial vessels and branches of the central artery of the retina. In the orbit, it has periaxial vessels from the ophthalmic artery and axial vessels from the central retinal artery. Within the cranium, it is supplied by the pial plexus fed by branches from the ophthalmic artery.
The pupil is a hole located in the centre of the iris that allows light to enter the retina. The iris contains muscles that control the size of the pupil in response to light and focusing. Anisocoria is when the pupils are unequal sizes and can be caused by physiological factors, trauma, inflammation, or neurological issues. Examining the pupils' reaction to light and focusing is important for evaluating eye and neurological function.
This document discusses the neural control mechanisms of eye movements. It describes three levels of control - supranuclear, nuclear, and infranuclear. At the supranuclear level, structures like the cerebral cortex, cerebellum, and brainstem nuclei control eye movements. The nuclear level includes brainstem nuclei that control the oculomotor cranial nerves. The infranuclear level involves the oculomotor nerves and extraocular muscles. There are two main types of eye movements - gaze shifting movements like saccades and smooth pursuit, and gaze holding movements like fixation and the vestibuloocular reflex. The document provides details on the neural circuits that generate and control different types of eye movements.
PATHWAY OF LIGHT REFLEX AND NEAR REFLEX.pptxSurabhi Deka
This document discusses the pathways of light reflex and near reflex in the eye. It begins by explaining how light reflex causes both pupils to constrict when light is shone in one eye. It then describes the pathway from the retina through the optic nerve, chiasm, and tract to the pretectal nucleus. It further explains how fibers from the pretectal nucleus connect to the Edinger-Westphal nucleus and travel along the oculomotor nerve to constrict the sphincter pupillae muscle. Abnormalities of the pathways such as afferent and efferent defects are also summarized, along with Adie's tonic pupil. In short, the document provides an overview of the neural pathways and functions of
Supranuclear disorders of ocular motilitySSSIHMS-PG
This document summarizes various disorders of ocular motility involving the supranuclear and internuclear pathways. It describes the different types of eye movements and their neural pathways/control centers in the brainstem. Key supranuclear disorders discussed include saccadic palsy, slowing of saccades in conditions like progressive supranuclear palsy, unwanted saccades like square wave jerks. Internuclear disorders summarized are internuclear ophthalmoplegia and skew deviation. Clinical features and localization of various vertical gaze palsies are also outlined.
The key arteries supplying the visual pathway include the internal carotid artery, posterior cerebral artery, anterior cerebral artery, ophthalmic artery, and posterior ciliary arteries. The central retinal artery supplies the retina. The optic nerve receives blood supply from the posterior ciliary arteries and branches of the ophthalmic artery. The optic chiasm, tract, lateral geniculate body, and visual cortex are supplied by branches of the internal carotid, anterior cerebral, and posterior cerebral arteries. Venous drainage is primarily through the central retinal vein, ophthalmic veins, basal veins and internal cerebral veins.
Saccadic eye movements are fast, conjugate movements that move both eyes quickly in the same direction to bring an object of interest onto the fovea. They have a peak velocity of 30-700 degrees per second and duration of 30-100 milliseconds. The latency between a target appearing and saccade onset is normally 150-250 milliseconds, but can be shorter for "express saccades". Saccades are controlled by burst neurons that generate a pulse to move the eyes rapidly, followed by tonic activity from step neurons to hold the eyes in place against elastic forces. Lesions in different brain regions involved in generating and modulating saccades can cause abnormalities such as slowed saccades, gaze-holding failure,
There are 6 extraocular muscles that control eye movement. The recti muscles rotate the eye in different directions while the oblique muscles cause torsional movement. Heterophoria is a latent misalignment of the eyes that is corrected by fusion. It can become manifest as a true strabismus. Comitant strabismus is when the eye deviation remains constant in all gazes, while incomitant strabismus involves restricted eye movement as well. Esotropia is inward eye turning and can be accommodative, non-accommodative, or secondary in nature.
This document discusses various types of ischemic optic neuropathy (ION). It begins by introducing ION as a major cause of vision loss and outlines its classification into anterior and posterior forms. It then details the anatomy and vascular supply of the optic nerve, risk factors for ION such as nocturnal blood pressure changes, and the pathogenesis involving hypoperfusion and axonal swelling. Non-arteritic anterior ION is described as the most common type, while posterior ION and arteritic forms are less prevalent but can involve vascular inflammation. The document outlines signs, investigations, management approaches including steroids, and variable prognoses for the different ION types.
This document provides an overview of the anatomy and microscopic structure of the retina. Key points include:
- The retina is a thin, delicate membrane lining the back of the eyeball. It contains photoreceptor cells (rods and cones) and neuronal layers.
- Gross anatomical regions include the optic disc, macula lutea, and peripheral retina. The macula contains the fovea centralis, which provides high-acuity central vision.
- Microscopically, the retina contains layers including the retinal pigment epithelium, photoreceptor outer and inner segments, plexiform layers, and ganglion cell layer.
- Rod and cone photoreceptors contain light-
The visual pathway begins in the retina and passes through the optic nerves, optic chiasm, and optic tracts to synapse in the lateral geniculate nucleus (LGN). From the LGN, fibers pass through the temporal and parietal lobes to terminate in the occipital lobes in the visual cortex. Lesions in different parts of the visual pathway can cause specific visual field defects, such as lesions of the optic nerve causing complete blindness in the affected eye.
This document provides descriptions of various ophthalmic signs, diseases, and findings using metaphorical descriptions. It describes signs related to the anterior segment such as seborrheic keratosis resembling a raspberry and chronic blepharitis resembling toothpaste. Posterior segment signs include amyloidosis resembling glass wool and proliferative sickle cell retinopathy resembling sea fans. Investigative findings include retinoblastoma resembling rosettes on histopathology and cuticular drusen resembling stars on fluorescein angiography. It also describes syndromes such as ablepharon-macrostomia resembling a fish mouse and pseudoxanthoma elasticum resembling a plucked chicken.
The optic nerve develops from the embryonic optic stalk and connects the optic vesicle to the forebrain. It begins forming in the 8th week of embryogenesis and myelination is completed shortly after birth. The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It transmits visual information from the retina to the brain and is supplied by branches from the ophthalmic artery and central retinal artery.
Primary optic atrophy occurs due to direct damage to the optic nerve and results in chalky white disc color with well defined margins and normal cupping and vessels. Secondary optic atrophy follows conditions like papilledema that cause swelling first, resulting in a filled cup and dirty white color. Consecutive optic atrophy occurs after other retinal conditions and shows waxy pallor, normal cup and grossly thinned vessels.
The document describes the neural pathway for vision, including the retina, optic nerve, optic tracts, lateral geniculate bodies, optic radiations, and visual cortex. It notes that the pathway involves three orders of neurons. It discusses how the nasal and temporal halves of the retina project to different sides of the brain, causing visual field defects when different areas are damaged. Common lesions that can cause visual field defects include those of the optic nerve, optic chiasm, optic tracts, lateral geniculate nucleus, optic radiations, and occipital lobe.
This document discusses the anatomy and manifestations of lesions along the visual pathway, including the optic nerve, chiasm, optic tract, lateral geniculate bodies, optic radiations, and visual cortex. Key points covered include the structures of each component of the visual pathway and the visual field defects that result from lesions in different locations, such as optic neuropathies, chiasmal syndromes, and homonymous hemianopsias from retrochiasmal lesions. Specific conditions like cortical blindness, dyschromatopsia, alexia without agraphia, and palinopsia that can arise from lesions in different areas are also mentioned.
The document summarizes the blood and nerve supply of the eye and optic nerve. It discusses the arterial supply which comes from branches of the internal and external carotid arteries. It then describes the specific branches like the central retinal artery and posterior ciliary arteries. It provides details on the venous drainage and nerve supply including the trigeminal, oculomotor, trochlear and abducent cranial nerves. In summary, it provides an overview of the arterial blood supply, venous drainage and cranial nerve innervation of the eye and optic nerve.
Direct Download Link ❤❤https://healthkura.com/eye-ppt/28/❤❤
Dear viewers Check Out my other piece of works at ❤❤❤ https://healthkura.com/eye-ppt/❤❤❤
anatomy of optic nerve and its blood supply and clinical corelation
Presentation Layout: optic nerve anatomy
Embryology of optic nerve
Introduction
Parts of optic nerve
Blood supply
Clinical significance
For Further Reading
Wolff’s Anatomy of the eye and orbit by Bron, Tripathi and Tripathi
Anatomy and Physiology of eye by A.K. Khurana 2nd edition
Comprehensive Ophthalmology by A.K. Khurana 5th edition
AAO- Fundamentals & Principles of Ophthalmology : sec 2
Walsh and Hoyt’s Clinical Ophthalmology
Internet
The optic nerve has no myelin sheath and is surrounded by meninges. It transmits signals from the retina and has four parts - intraocular, intraorbital, canalicular, and intracranial. The optic nerve head contains zones like the superficial nerve fiber layer, prelaminar zone, lamina cribrosa, and retrolaminar region. The lamina cribrosa provides a blood supply and the nerve increases in diameter after passing through it. In glaucoma, retinal ganglion cell loss leads to cupping of the optic disc. The optic nerve receives blood supply from the ophthalmic and ciliary arteries. Dysfunctions can cause visual field defects, changes to acuity and
The document discusses visual field testing techniques including kinetic methods using moving targets and static methods using stationary targets. It describes common visual field parameters like isopters and various pathologies that can cause visual field defects like glaucoma. Standardized tests are discussed including the tangent screen test and different algorithms used for static threshold tests like SITA. Key aspects of visual field analyzer equipment and reliable interpretation of results are also covered.
The optic nerve develops from the embryonic optic stalk and contains axons originating from retinal ganglion cells. It has intraocular, intraorbital, intracanalicular, and intracranial parts. The intraocular part passes through the lamina cribrosa and expands as it acquires a myelin sheath. The optic nerve receives its blood supply from short posterior ciliary arteries and pial vessels.
The optic nerve receives its blood supply from multiple sources along its path from the eye to the brain. In the eye, it is supplied by retinal arterioles and occasionally the ciliary artery. In the prelaminar region, it receives blood from ciliary region vessels and peripapillary choroidal or short posterior ciliary vessels. Deeper regions receive supply from ciliary and retinal circulations, including recurrent pial vessels and branches of the central artery of the retina. In the orbit, it has periaxial vessels from the ophthalmic artery and axial vessels from the central retinal artery. Within the cranium, it is supplied by the pial plexus fed by branches from the ophthalmic artery.
The pupil is a hole located in the centre of the iris that allows light to enter the retina. The iris contains muscles that control the size of the pupil in response to light and focusing. Anisocoria is when the pupils are unequal sizes and can be caused by physiological factors, trauma, inflammation, or neurological issues. Examining the pupils' reaction to light and focusing is important for evaluating eye and neurological function.
This document discusses the neural control mechanisms of eye movements. It describes three levels of control - supranuclear, nuclear, and infranuclear. At the supranuclear level, structures like the cerebral cortex, cerebellum, and brainstem nuclei control eye movements. The nuclear level includes brainstem nuclei that control the oculomotor cranial nerves. The infranuclear level involves the oculomotor nerves and extraocular muscles. There are two main types of eye movements - gaze shifting movements like saccades and smooth pursuit, and gaze holding movements like fixation and the vestibuloocular reflex. The document provides details on the neural circuits that generate and control different types of eye movements.
PATHWAY OF LIGHT REFLEX AND NEAR REFLEX.pptxSurabhi Deka
This document discusses the pathways of light reflex and near reflex in the eye. It begins by explaining how light reflex causes both pupils to constrict when light is shone in one eye. It then describes the pathway from the retina through the optic nerve, chiasm, and tract to the pretectal nucleus. It further explains how fibers from the pretectal nucleus connect to the Edinger-Westphal nucleus and travel along the oculomotor nerve to constrict the sphincter pupillae muscle. Abnormalities of the pathways such as afferent and efferent defects are also summarized, along with Adie's tonic pupil. In short, the document provides an overview of the neural pathways and functions of
Supranuclear disorders of ocular motilitySSSIHMS-PG
This document summarizes various disorders of ocular motility involving the supranuclear and internuclear pathways. It describes the different types of eye movements and their neural pathways/control centers in the brainstem. Key supranuclear disorders discussed include saccadic palsy, slowing of saccades in conditions like progressive supranuclear palsy, unwanted saccades like square wave jerks. Internuclear disorders summarized are internuclear ophthalmoplegia and skew deviation. Clinical features and localization of various vertical gaze palsies are also outlined.
The key arteries supplying the visual pathway include the internal carotid artery, posterior cerebral artery, anterior cerebral artery, ophthalmic artery, and posterior ciliary arteries. The central retinal artery supplies the retina. The optic nerve receives blood supply from the posterior ciliary arteries and branches of the ophthalmic artery. The optic chiasm, tract, lateral geniculate body, and visual cortex are supplied by branches of the internal carotid, anterior cerebral, and posterior cerebral arteries. Venous drainage is primarily through the central retinal vein, ophthalmic veins, basal veins and internal cerebral veins.
Saccadic eye movements are fast, conjugate movements that move both eyes quickly in the same direction to bring an object of interest onto the fovea. They have a peak velocity of 30-700 degrees per second and duration of 30-100 milliseconds. The latency between a target appearing and saccade onset is normally 150-250 milliseconds, but can be shorter for "express saccades". Saccades are controlled by burst neurons that generate a pulse to move the eyes rapidly, followed by tonic activity from step neurons to hold the eyes in place against elastic forces. Lesions in different brain regions involved in generating and modulating saccades can cause abnormalities such as slowed saccades, gaze-holding failure,
There are 6 extraocular muscles that control eye movement. The recti muscles rotate the eye in different directions while the oblique muscles cause torsional movement. Heterophoria is a latent misalignment of the eyes that is corrected by fusion. It can become manifest as a true strabismus. Comitant strabismus is when the eye deviation remains constant in all gazes, while incomitant strabismus involves restricted eye movement as well. Esotropia is inward eye turning and can be accommodative, non-accommodative, or secondary in nature.
This document discusses various types of ischemic optic neuropathy (ION). It begins by introducing ION as a major cause of vision loss and outlines its classification into anterior and posterior forms. It then details the anatomy and vascular supply of the optic nerve, risk factors for ION such as nocturnal blood pressure changes, and the pathogenesis involving hypoperfusion and axonal swelling. Non-arteritic anterior ION is described as the most common type, while posterior ION and arteritic forms are less prevalent but can involve vascular inflammation. The document outlines signs, investigations, management approaches including steroids, and variable prognoses for the different ION types.
This document provides an overview of the anatomy and microscopic structure of the retina. Key points include:
- The retina is a thin, delicate membrane lining the back of the eyeball. It contains photoreceptor cells (rods and cones) and neuronal layers.
- Gross anatomical regions include the optic disc, macula lutea, and peripheral retina. The macula contains the fovea centralis, which provides high-acuity central vision.
- Microscopically, the retina contains layers including the retinal pigment epithelium, photoreceptor outer and inner segments, plexiform layers, and ganglion cell layer.
- Rod and cone photoreceptors contain light-
The visual pathway begins in the retina and passes through the optic nerves, optic chiasm, and optic tracts to synapse in the lateral geniculate nucleus (LGN). From the LGN, fibers pass through the temporal and parietal lobes to terminate in the occipital lobes in the visual cortex. Lesions in different parts of the visual pathway can cause specific visual field defects, such as lesions of the optic nerve causing complete blindness in the affected eye.
This document provides descriptions of various ophthalmic signs, diseases, and findings using metaphorical descriptions. It describes signs related to the anterior segment such as seborrheic keratosis resembling a raspberry and chronic blepharitis resembling toothpaste. Posterior segment signs include amyloidosis resembling glass wool and proliferative sickle cell retinopathy resembling sea fans. Investigative findings include retinoblastoma resembling rosettes on histopathology and cuticular drusen resembling stars on fluorescein angiography. It also describes syndromes such as ablepharon-macrostomia resembling a fish mouse and pseudoxanthoma elasticum resembling a plucked chicken.
The optic nerve develops from the embryonic optic stalk and connects the optic vesicle to the forebrain. It begins forming in the 8th week of embryogenesis and myelination is completed shortly after birth. The optic nerve has four parts - intraocular, intraorbital, intracanalicular, and intracranial. It transmits visual information from the retina to the brain and is supplied by branches from the ophthalmic artery and central retinal artery.
The ophthalmic artery originates from the internal carotid artery as it leaves the cavernous sinus. It passes through the optic canal and orbits the eye, dividing into branches that supply the eye and surrounding structures. The central artery of the retina arises in the optic canal and supplies the retina. The lacrimal artery runs to the lacrimal gland. Other branches include the supraorbital, anterior and posterior ethmoidal, meningeal, muscular, and dorsal nasal and supratrochlear arteries which supply the surrounding areas. The ciliary arteries pierce the sclera to supply the choroid, iris, and ciliary body. The ophthalmic artery and its branches provide the main blood supply to
This document provides descriptions of various ophthalmic signs and findings, organized by anatomical location. In 3 sentences:
It lists over 30 signs seen in the anterior and posterior segments of the eye, such as the "setting sun" appearance seen in infantile hydrocephalus and "snowflake cataract". Investigative tests are also described, like the "collar-stud" appearance of choroidal melanoma on US B-scan and various patterns seen on fluorescein angiography like the "smoke-stack" in central serous retinopathy. The document aims to familiarize readers with clinical signs seen around the eye through descriptive names and images.
This document discusses various classes of antibiotics used in oral and maxillofacial surgery. It begins by describing the classification, mechanisms of action, spectra of activity, uses and side effects of different antibiotic classes including sulfonamides, quinolones, beta-lactams, tetracyclines, aminoglycosides, macrolides and more. It provides details on specific antibiotics within each class, along with their dosages and trade names. The document serves as a comprehensive reference for oral and maxillofacial surgeons on the properties and clinical applications of numerous antibiotics.
The abducens nerve originates in the pons and contains motor neurons that innervate the lateral rectus muscle, allowing for eye movement outward. It exits the brainstem and travels through the cavernous sinus before entering the orbit through the superior orbital fissure to innervate the lateral rectus. Pathologies of the abducens nerve can occur at the nuclear, central, cisternal, petrous, cavernous, or orbital segments and result in lateral rectus palsy and limitations in abduction of the eye. Common causes include pontine hemorrhage, MS, meningiomas, and traumatic injuries.
This document discusses two antiviral medications - acyclovir and ritonavir. Acyclovir is used to treat infections caused by herpes viruses, such as genital herpes and shingles. It works by inhibiting viral replication. Ritonavir is used to treat HIV infection in combination with other antiretroviral agents. It prevents HIV from multiplying in the body. Both medications have potential side effects and require careful administration according to prescribed dosages and schedules. Nursing responsibilities for the two drugs include monitoring for side effects, ensuring proper administration, and patient education.
The trochlear nerve has a sole function of innervating the superior oblique muscle of the contralateral orbit. It originates from the trochlear nucleus in the midbrain and travels through the cistern, cavernous sinus, and superior orbital fissure before innervating the superior oblique muscle. Damage to different segments of the trochlear nerve can result in various clinical presentations including superior oblique palsy and diplopia.
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This document discusses principles of antibiotic therapy in ophthalmology. It outlines different classes of antibiotics including penicillins, cephalosporins, aminoglycosides, macrolides, chloramphenicol, and fluoroquinolones. It describes how each class works and common pathogens they target. Dangers of antibiotic overuse like bacterial resistance and toxicity are also covered. The document provides guidance on selecting antibiotics based on the organism, disease severity, and patient factors. It concludes by describing various methods of antibiotic administration for ophthalmic conditions like topical, subconjunctival, intracameral, and systemic delivery.
This document discusses antibiotic ocular drugs, including their modes of administration, guidelines for effective use, reasons for treatment failure, and relationship to bacterial structure. It covers various classes of antibiotics like penicillins, cephalosporins, aminoglycosides, fluoroquinolones and their mechanisms of action, clinical uses, side effects and contraindications. The presentation provides an overview of antibiotic ocular drug therapy and factors influencing treatment effectiveness.
This PowerPoint presentation covers the history and mechanisms of antimicrobial drugs. It discusses:
1) The contributions of Paul Ehrlich and Alexander Fleming to chemotherapy through the discovery of selective toxicity and penicillin.
2) The major classes of antimicrobial drugs like antibiotics, antifungals, antivirals, and their mechanisms of action including inhibiting cell wall, protein, and nucleic acid synthesis.
3) Specific drugs for bacteria, mycobacteria, fungi, viruses, protozoa and helminths from each class and their targets in the microbe.
4) Issues with developing drugs given differences between microbial and human cells, and the growing problem of antimicrobial resistance.
This document contains a PowerPoint presentation on viruses, viroids, and prions. It discusses the general characteristics of viruses, including that they are obligate intracellular parasites that require a living host cell to multiply. It also covers viral structure, taxonomy, isolation/cultivation methods, and viral multiplication cycles. Specifically, it describes the lytic and lysogenic cycles of bacteriophages, as well as the replication cycles of DNA and RNA containing animal viruses. Key aspects of viral structure and replication are illustrated with diagrams.
Fungal infections of eye cause one of the most dangerious infections. Accurate diagnosis and proper institution of anti-fungal therapy is essential. Here we discuss the various anti-fungal agents available to be used in ophthalmology.
The document discusses eye movement control systems in humans. It describes the different types of eye movements including saccades, smooth pursuit, optokinetic, and vestibulo-ocular reflexes. It outlines the major brainstem control centers involved including the PPRF, riMLF, MLF, vestibular nuclei, and cerebellum. Supranuclear control is provided by the frontal eye fields, parieto-occipital junction, and superior colliculus. Common eye movement disorders are also summarized.
ocular pharmacology anti viral and anti fungalPratyush Dhakal
This document discusses antiviral and antifungal drugs used in ophthalmology. It begins by defining antiviral drugs and their mechanisms of action, then lists specific antiviral drugs used to treat various viral infections affecting the eye, including herpes simplex virus, herpes zoster virus, and cytomegalovirus. It discusses the mechanisms and uses of common antiviral drugs like acyclovir, vidarabine, ganciclovir. The document also covers major classes of antifungal drugs including polyenes, imidazoles, and their mechanisms and specific drugs used to treat fungal infections like natamycin, amphotericin B, miconazole.
This document provides information on the anatomy and physiology of the pupil, including:
- The normal features of a pupil such as size, shape, number, location and color.
- The sphincter pupillae and dilator pupillae muscles that control pupil size and their innervation by the parasympathetic and sympathetic nervous systems.
- Pupillary reflexes including the light reflex, near reflex and darkness reflex and their neural pathways.
- Abnormal pupils including causes of anisocoria, leukocoria and variations in shape, size and location.
This document discusses supranuclear pathways and lesions that can affect eye movements. It begins with the fundamentals of extraocular movements and anatomy of cortical and brainstem centers that control eye movements. It then covers the basic types of eye movements like saccades, smooth pursuit, vestibular-ocular reflex, and vergence movements. It provides a step-wise approach to evaluating eye movement disorders and localizing lesions based on the type of eye movement affected. Supranuclear lesions can cause bilateral eye movement involvement, while specific brainstem lesions impact horizontal or vertical eye movements or specific eye movement types like saccades or vestibular-ocular reflex.
This document discusses various antiviral drugs used to treat viral eye infections caused by DNA and RNA viruses such as herpes simplex virus and cytomegalovirus. It describes first and second generation antiviral drugs such as trifluorothymidine, acyclovir, ganciclovir and foscarnet. It provides details on the mechanisms of action, indications, dosages and side effects of these drugs for treating ocular conditions.
Localizing signs for lesion of visual pathwaySiva G
1. Lesions along the visual pathway can be localized based on the type of visual field defect they cause.
2. Pre-chiasmal lesions cause unilateral visual field defects respecting the horizontal meridian, chiasmal lesions cause non-homonymous defects, and post-chiasmal lesions cause homonymous defects respecting the vertical meridian.
3. Specific lesions like optic nerve lesions or craniopharyngiomas cause characteristic visual field defects that can help localize the lesion location. Visual field testing is an important tool to localize lesions along the visual pathway.
This document provides an overview of neuro-opthalmology, including:
- The anatomy and blood supply of the visual pathway from the optic nerve to the lateral geniculate nucleus.
- Common causes of ischemic optic neuropathy and optic neuritis.
- Localization of different visual field defects based on lesion location.
- Syndromes associated with occipital lobe lesions like Anton syndrome and Balint's syndrome.
- Causes and localization of different types of nystagmus and motility disturbances.
- Pupillary abnormalities and their causes like Horner syndrome and Argyll Robertson pupils.
This document discusses visual pathway anatomy and lesions that can occur along the visual pathway. It describes the components of the visual pathway, including the optic nerve, optic chiasm, optic tracts, lateral geniculate bodies, and optic radiations. It details the types of field defects that can result from lesions in each of these areas, such as hemianopia from optic chiasm lesions or quadrantanopia from optic tract lesions. Common causes of lesions are also outlined for each part of the visual pathway. Clinical features of different lesions are compared.
This document provides an overview of optic neuropathies. It begins by defining optic neuropathies as disorders of the optic nerve and describes their clinical presentations. It then discusses various mechanisms and types of optic neuropathies including ischemic, compressive, infiltrative, and hereditary. Specific conditions like anterior ischemic optic neuropathy (AION), giant cell arteritis, optic neuritis, and Leber's hereditary optic neuropathy are described. Diagnostic testing and treatment approaches are also summarized for different optic neuropathies.
The document discusses the human visual system and methods for clinical assessment of visual function. It describes the pathway from the retina through the optic nerve, optic chiasm, optic tract, lateral geniculate body, and primary visual cortex. It also details the pupil response pathway and methods to test visual acuity, color vision, eye movements, stereopsis, and visual fields. Common refractive errors and disorders that can be identified through clinical assessment are outlined.
This document provides an overview of the anatomy and clinical assessment of the optic nerve in 3 paragraphs:
1) It describes the anatomy of the optic nerve, including its origin from the ganglion cells and path from the optic disc to the optic chiasm. It is composed of over 1 million axons and is divided into intraocular, intraorbital, intracanalicular, and intracranial portions.
2) Clinical assessment of the optic nerve involves testing visual acuity, color vision, visual fields, and the pupillary light reflex. Signs of optic nerve pathology include an afferent pupillary defect.
3) Different pathologies like papilledema, optic neuritis, and optic
This document discusses the differential diagnosis and examination for patients presenting with sudden visual loss. It covers common causes grouped by duration of symptoms and presence of pain. Causes include retinal vascular diseases like retinal vein occlusion, optic neuropathies, and conditions affecting the retina such as macular hole and retinal detachment. Examination tests like visual acuity, visual fields, and fundus examination are important for determining the cause. A case study example is also provided of a patient diagnosed with non-arteritic anterior ischemic optic neuropathy based on symptoms and examination findings.
Clinical approach to optic neuropathies dove med pressneurophq8
This document provides an overview of the clinical approach to diagnosing various types of optic neuropathies. It discusses the importance of obtaining a thorough history and performing a neuro-ophthalmic examination to identify signs of optic neuropathy. Ancillary testing like visual field testing, electrophysiology, and optical coherence tomography can aid diagnosis. The document then reviews the diagnostic criteria and approach to specific optic neuropathies like acute demyelinating optic neuritis.
Refractive errors of eye ophthalmology astigmatism hypermetropia myopia medic...TONY SCARIA
This document discusses various refractive errors of the eye including emmetropia, ametropia, myopia, hypermetropia, and astigmatism. It provides details on the etiology, classification, signs, symptoms, and treatment options for each condition. Key points include:
- Myopia is caused by the eyeball being too long or the cornea having too much curvature. It is usually treated with concave glasses, contact lenses, or refractive surgery like LASIK.
- Hypermetropia is caused by the eyeball being too short or the cornea having too weak curvature. It can be corrected with convex glasses, contact lenses, or refractive procedures.
- Astig
This document provides an overview of evaluating and classifying decreased vision. It discusses evaluating the history, color vision, pupils, fundus, visual fields, and ancillary tests. It then classifies causes as macular, retinal, optic neuropathy, chiasmopathy, visual pathway, or occipital cortex. Specific conditions discussed include NAION, Leber's hereditary optic neuropathy, compressive optic neuropathies, toxic/nutritional neuropathies, and lesions of the chiasm, optic tract, lateral geniculate, and occipital cortex.
1. The visual pathway includes the optic nerve, optic chiasm, optic tracts, lateral geniculate bodies, and optic radiations which transmit visual information from the eyes to the visual cortex.
2. Lesions along the visual pathway can cause different types of visual field defects including hemianopia, quadrantanopia, and homonymous hemianopia. The type and characteristics of the field defect depend on the specific location of the lesion.
3. Pupillary reflexes involve both afferent and efferent pathways. Abnormalities of the pupillary reflexes can localize lesions and help diagnose conditions affecting the visual pathway or autonomic nervous system.
This document provides an overview of optic atrophy, including:
1. It defines optic atrophy as degeneration of the optic nerve due to damage to the visual pathways from the retina to the lateral geniculate body.
2. It classifies optic atrophy based on whether damage originates in the retina or more centrally, and by cause. Primary optic atrophy occurs without swelling, while secondary involves prior swelling.
3. Causes of primary optic atrophy include optic neuritis, compression, hereditary conditions, toxins, trauma, and multiple sclerosis. Secondary optic atrophy follows conditions like papilledema.
4. Treatment focuses on the underlying cause, with vitamins sometimes used
This document discusses optic nerve disease and optic neuropathy. It covers the clinical features, examination, investigations, and various causes of optic nerve disease including optic neuritis, nutritional optic neuropathy, anterior ischemic optic neuropathy, papilledema, and Leber's hereditary optic neuropathy. Examinations discussed include visual acuity testing, color vision testing, visual field testing, ophthalmoscopy, fluorescein angiography, and visual evoked potentials. Causes covered in more depth include optic neuritis, anterior ischemic optic neuropathy, nutritional optic neuropathy, papilledema, and Leber's hereditary optic neuropathy.
The document discusses various retinal conditions and diseases. It provides information on symptoms, clinical findings, inheritance patterns, pathophysiology and testing results for each condition. These include congenital stationary night blindness, fundus albipunctatus, retinitis pigmentosa, cone dystrophy, Stargardt disease, Best disease, gyrate atrophy, choroideremia, juvenile retinoschisis, Bardet-Biedl syndrome, Tay-Sachs disease, Bietti’s crystalline retinopathy and others. It also covers post-traumatic conditions like commotio retinae, choroidal rupture, intraocular foreign bodies, shaken baby syndrome and Valsalva retinopathy.
This document discusses defects of the visual pathway, including definitions of visual fields and how they are mapped. It describes how the image is inverted on the retina. Various types of visual field defects are defined such as scotomas, quadrantanopias, and hemianopias. Lesions along different parts of the visual pathway are described, including lesions of the optic nerve, optic chiasm, optic tract, lateral geniculate body, optic radiations, and visual cortex. The characteristics and causes of visual field defects resulting from lesions in each of these areas are provided.
This document discusses myopia (nearsightedness), including its classification, grading, clinical varieties, etiology, signs and symptoms, and treatment options. Myopia occurs when parallel rays of light focus in front of the retina, in contrast to emmetropia where the focus is on the retina. It is classified by etiology such as axial or curvatural myopia. Treatment includes optical options like glasses/contacts and surgical procedures like LASIK. Preventive measures aim to slow progression by reducing near work and increasing outdoor activity.
This document discusses lesions in the occipital lobe and their effects. It covers topics such as field defects from lesions of the primary visual cortex, including homonymous hemianopia. It also discusses cortical blindness, Anton's syndrome, and other syndromes. Lesions of the ventral stream can cause visual agnosias like object agnosia and prosopagnosia. Disorders of the dorsal stream include Balint's syndrome and simultanagnosia. Various visual hallucinations and other positive visual phenomena are also covered. The document provides detailed information on the anatomical localization and clinical features of different visual disorders.
This document provides information about ectopia lentis, or displacement of the crystalline lens. It begins with classifications of ectopia lentis based on location and etiology. Congenital causes like Marfan syndrome and homocystinuria are described. Presentation, examination findings, complications, workup, and management approaches are outlined. Surgical techniques depend on degree and location of lens subluxation/dislocation and may involve lens removal with or without intraocular lens implantation. Management of subluxated lenses in children poses additional challenges due to risk of complications with contact lenses or suture-fixated intraocular lenses.
This document provides information on ectopia lentis, or displacement of the crystalline lens. It begins with classifications of ectopia lentis based on location and etiology. Congenital causes such as Marfan syndrome and homocystinuria are described. Traumatic and spontaneous dislocation are also discussed. Presentation, examination findings, complications, workup, and management approaches such as surgery and devices like capsular tension rings are outlined. Key surgical techniques for addressing subluxated or dislocated lenses are presented. Management in children poses additional challenges.
Nutritional deficiency Disorder are problems in india.
It is very important to learn about Indian child's nutritional parameters as well the Disease related to alteration in their Nutrition.
Osvaldo Bernardo Muchanga-GASTROINTESTINAL INFECTIONS AND GASTRITIS-2024.pdfOsvaldo Bernardo Muchanga
GASTROINTESTINAL INFECTIONS AND GASTRITIS
Osvaldo Bernardo Muchanga
Gastrointestinal Infections
GASTROINTESTINAL INFECTIONS result from the ingestion of pathogens that cause infections at the level of this tract, generally being transmitted by food, water and hands contaminated by microorganisms such as E. coli, Salmonella, Shigella, Vibrio cholerae, Campylobacter, Staphylococcus, Rotavirus among others that are generally contained in feces, thus configuring a FECAL-ORAL type of transmission.
Among the factors that lead to the occurrence of gastrointestinal infections are the hygienic and sanitary deficiencies that characterize our markets and other places where raw or cooked food is sold, poor environmental sanitation in communities, deficiencies in water treatment (or in the process of its plumbing), risky hygienic-sanitary habits (not washing hands after major and/or minor needs), among others.
These are generally consequences (signs and symptoms) resulting from gastrointestinal infections: diarrhea, vomiting, fever and malaise, among others.
The treatment consists of replacing lost liquids and electrolytes (drinking drinking water and other recommended liquids, including consumption of juicy fruits such as papayas, apples, pears, among others that contain water in their composition).
To prevent this, it is necessary to promote health education, improve the hygienic-sanitary conditions of markets and communities in general as a way of promoting, preserving and prolonging PUBLIC HEALTH.
Gastritis and Gastric Health
Gastric Health is one of the most relevant concerns in human health, with gastrointestinal infections being among the main illnesses that affect humans.
Among gastric problems, we have GASTRITIS AND GASTRIC ULCERS as the main public health problems. Gastritis and gastric ulcers normally result from inflammation and corrosion of the walls of the stomach (gastric mucosa) and are generally associated (caused) by the bacterium Helicobacter pylor, which, according to the literature, this bacterium settles on these walls (of the stomach) and starts to release urease that ends up altering the normal pH of the stomach (acid), which leads to inflammation and corrosion of the mucous membranes and consequent gastritis or ulcers, respectively.
In addition to bacterial infections, gastritis and gastric ulcers are associated with several factors, with emphasis on prolonged fasting, chemical substances including drugs, alcohol, foods with strong seasonings including chilli, which ends up causing inflammation of the stomach walls and/or corrosion. of the same, resulting in the appearance of wounds and consequent gastritis or ulcers, respectively.
Among patients with gastritis and/or ulcers, one of the dilemmas is associated with the foods to consume in order to minimize the sensation of pain and discomfort.
The Children are very vulnerable to get affected with respiratory disease.
In our country, the respiratory Disease conditions are consider as major cause for mortality and Morbidity in Child.
5-hydroxytryptamine or 5-HT or Serotonin is a neurotransmitter that serves a range of roles in the human body. It is sometimes referred to as the happy chemical since it promotes overall well-being and happiness.
It is mostly found in the brain, intestines, and blood platelets.
5-HT is utilised to transport messages between nerve cells, is known to be involved in smooth muscle contraction, and adds to overall well-being and pleasure, among other benefits. 5-HT regulates the body's sleep-wake cycles and internal clock by acting as a precursor to melatonin.
It is hypothesised to regulate hunger, emotions, motor, cognitive, and autonomic processes.
PGx Analysis in VarSeq: A User’s PerspectiveGolden Helix
Since our release of the PGx capabilities in VarSeq, we’ve had a few months to gather some insights from various use cases. Some users approach PGx workflows by means of array genotyping or what seems to be a growing trend of adding the star allele calling to the existing NGS pipeline for whole genome data. Luckily, both approaches are supported with the VarSeq software platform. The genotyping method being used will also dictate what the scope of the tertiary analysis will be. For example, are your PGx reports a standalone pipeline or would your lab’s goal be to handle a dual-purpose workflow and report on PGx + Diagnostic findings.
The purpose of this webcast is to:
Discuss and demonstrate the approaches with array and NGS genotyping methods for star allele calling to prep for downstream analysis.
Following genotyping, explore alternative tertiary workflow concepts in VarSeq to handle PGx reporting.
Moreover, we will include insights users will need to consider when validating their PGx workflow for all possible star alleles and options you have for automating your PGx analysis for large number of samples. Please join us for a session dedicated to the application of star allele genotyping and subsequent PGx workflows in our VarSeq software.
Nano-gold for Cancer Therapy chemistry investigatory projectSIVAVINAYAKPK
chemistry investigatory project
The development of nanogold-based cancer therapy could revolutionize oncology by providing a more targeted, less invasive treatment option. This project contributes to the growing body of research aimed at harnessing nanotechnology for medical applications, paving the way for future clinical trials and potential commercial applications.
Cancer remains one of the leading causes of death worldwide, prompting the need for innovative treatment methods. Nanotechnology offers promising new approaches, including the use of gold nanoparticles (nanogold) for targeted cancer therapy. Nanogold particles possess unique physical and chemical properties that make them suitable for drug delivery, imaging, and photothermal therapy.
Giloy in Ayurveda - Classical Categorization and SynonymsPlanet Ayurveda
Giloy, also known as Guduchi or Amrita in classical Ayurvedic texts, is a revered herb renowned for its myriad health benefits. It is categorized as a Rasayana, meaning it has rejuvenating properties that enhance vitality and longevity. Giloy is celebrated for its ability to boost the immune system, detoxify the body, and promote overall wellness. Its anti-inflammatory, antipyretic, and antioxidant properties make it a staple in managing conditions like fever, diabetes, and stress. The versatility and efficacy of Giloy in supporting health naturally highlight its importance in Ayurveda. At Planet Ayurveda, we provide a comprehensive range of health services and 100% herbal supplements that harness the power of natural ingredients like Giloy. Our products are globally available and affordable, ensuring that everyone can benefit from the ancient wisdom of Ayurveda. If you or your loved ones are dealing with health issues, contact Planet Ayurveda at 01725214040 to book an online video consultation with our professional doctors. Let us help you achieve optimal health and wellness naturally.
The skin is the largest organ and its health plays a vital role among the other sense organs. The skin concerns like acne breakout, psoriasis, or anything similar along the lines, finding a qualified and experienced dermatologist becomes paramount.
Debunking Nutrition Myths: Separating Fact from Fiction"AlexandraDiaz101
In a world overflowing with diet trends and conflicting nutrition advice, it’s easy to get lost in misinformation. This article cuts through the noise to debunk common nutrition myths that may be sabotaging your health goals. From the truth about carbohydrates and fats to the real effects of sugar and artificial sweeteners, we break down what science actually says. Equip yourself with knowledge to make informed decisions about your diet, and learn how to navigate the complexities of modern nutrition with confidence. Say goodbye to food confusion and hello to a healthier you!
- Video recording of this lecture in English language: https://youtu.be/Pt1nA32sdHQ
- Video recording of this lecture in Arabic language: https://youtu.be/uFdc9F0rlP0
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Breast cancer: Post menopausal endocrine therapyDr. Sumit KUMAR
Breast cancer in postmenopausal women with hormone receptor-positive (HR+) status is a common and complex condition that necessitates a multifaceted approach to management. HR+ breast cancer means that the cancer cells grow in response to hormones such as estrogen and progesterone. This subtype is prevalent among postmenopausal women and typically exhibits a more indolent course compared to other forms of breast cancer, which allows for a variety of treatment options.
Diagnosis and Staging
The diagnosis of HR+ breast cancer begins with clinical evaluation, imaging, and biopsy. Imaging modalities such as mammography, ultrasound, and MRI help in assessing the extent of the disease. Histopathological examination and immunohistochemical staining of the biopsy sample confirm the diagnosis and hormone receptor status by identifying the presence of estrogen receptors (ER) and progesterone receptors (PR) on the tumor cells.
Staging involves determining the size of the tumor (T), the involvement of regional lymph nodes (N), and the presence of distant metastasis (M). The American Joint Committee on Cancer (AJCC) staging system is commonly used. Accurate staging is critical as it guides treatment decisions.
Treatment Options
Endocrine Therapy
Endocrine therapy is the cornerstone of treatment for HR+ breast cancer in postmenopausal women. The primary goal is to reduce the levels of estrogen or block its effects on cancer cells. Commonly used agents include:
Selective Estrogen Receptor Modulators (SERMs): Tamoxifen is a SERM that binds to estrogen receptors, blocking estrogen from stimulating breast cancer cells. It is effective but may have side effects such as increased risk of endometrial cancer and thromboembolic events.
Aromatase Inhibitors (AIs): These drugs, including anastrozole, letrozole, and exemestane, lower estrogen levels by inhibiting the aromatase enzyme, which converts androgens to estrogen in peripheral tissues. AIs are generally preferred in postmenopausal women due to their efficacy and safety profile compared to tamoxifen.
Selective Estrogen Receptor Downregulators (SERDs): Fulvestrant is a SERD that degrades estrogen receptors and is used in cases where resistance to other endocrine therapies develops.
Combination Therapies
Combining endocrine therapy with other treatments enhances efficacy. Examples include:
Endocrine Therapy with CDK4/6 Inhibitors: Palbociclib, ribociclib, and abemaciclib are CDK4/6 inhibitors that, when combined with endocrine therapy, significantly improve progression-free survival in advanced HR+ breast cancer.
Endocrine Therapy with mTOR Inhibitors: Everolimus, an mTOR inhibitor, can be added to endocrine therapy for patients who have developed resistance to aromatase inhibitors.
Chemotherapy
Chemotherapy is generally reserved for patients with high-risk features, such as large tumor size, high-grade histology, or extensive lymph node involvement. Regimens often include anthracyclines and taxanes.
2. Contents
Definition of visual field
Normal vision
What are the causes of visual field defect?
Anatomy of Visual pathways
Optic nerve
Optic chiasm
Retrochiasm
Visual field deficits due to various lesions.
How to approach a patient with specific visual field deficit ?
Optic neuropathies
Summary
3. VISUAL FIELD
“A space in the universe, visiblle to steadily fixating eye”
4. CAUSES OF FIELD DEFECTS
Media opacity
Retinal Pathologies
Visual pathway lesions
Cortical lesions
5. RETINAL VS NEUROLOGICAL CAUSES
Retinal causes respect the horizontal midline
Neurological causes respect the vertical midline
33. Patient with contralateral superior
quadrantanopia
Associaed features
C/L hemisensory loss and hemiparesis
Paroxysmal olfactory and gustatory hallucinations
Formed visual hallucinations
Seizures
Receptive dysphasia(Dominat hemisphere)
34.
35. Patient presenting with
contralateral inferior qurantanopia
Associated feature
Acalculia, Agraphia,left-right disorientation and finger agnosia
Dressing and constitutional apraxia , spatial neglect
38. Parietal Vs Occipital Lobe lesions
Jerky movements induced by moving
pattern targets across the visual field
Parietal lobe lesion: asymmetric OKN
(Slow pursuit movements are affected)
Occipital lobe lesions: Symmetric OKN
Parietal lobe lesions are more likely to be a
tumor while occipital lobe lesions are more likely
to be infarction
39. Optic nerve neuropathies
Symptoms of optic nerve dysfunction
Visual loss
Dark adaptation is lowered
Impaired color vision
Transient obscuration of vision
Depth perception is impaired
Pain : mild dull eye ache
40. Signs Of Optic nerve dysfunction
Decreased VA
RAPD
Dyschromatopsia
Diminished light brightness sensitivity
Deminished contrast sensitivity
Visual field defects
42. Optic Atrophy
Primary optic atrophy
Changes that take place in the optic nerve due to axonal degeneration in the pathway
b/w retina and LGB
Secondary optic atrophy
43. Optic neuritis
Retrobulbar optic neuritis : Most commonly associated with MS
Papillitis : inflammation of intraocular portion of optic nerve
Neroretinitis: Papillitis in association with inflammation of RNFL and a
MACULAR STAR
“Inflammation of optic nerve is called optic neuritis”
Papillitis Neuroretinitis