The document provides information on techniques for examining the eye, including:
1. Visual acuity is tested using a Snellen eye chart from 20 feet.
2. Visual fields are assessed using confrontation tests like finger wiggling.
3. The optic disc, retina, blood vessels and macula are examined using an ophthalmoscope.
Head (Skull, Scalp, Hair)
Face
Eyebrows, Eyes and Eyelashes
Eye lids and Lacrimal Apparatus
Conjunctivae
Sclerae
Cornea
Anterior Chamber and Iris
Pupils
Cranial Nerve II (optic nerve)
Cranial Nerve III, IV & VI (Oculomotor, Trochlear, Abducens)
Ears
Nose and Paranasal Sinuses
Cranial Nerve I (olfactory Nerve)
Neck
Thorax ( Cardiovascular System)
Breast
Abdomen
Extremities
Head (Skull, Scalp, Hair)
Face
Eyebrows, Eyes and Eyelashes
Eye lids and Lacrimal Apparatus
Conjunctivae
Sclerae
Cornea
Anterior Chamber and Iris
Pupils
Cranial Nerve II (optic nerve)
Cranial Nerve III, IV & VI (Oculomotor, Trochlear, Abducens)
Ears
Nose and Paranasal Sinuses
Cranial Nerve I (olfactory Nerve)
Neck
Thorax ( Cardiovascular System)
Breast
Abdomen
Extremities
General Physical Examination is an essential part of all the examinations of human body. a brief knowledge of every step of this examination must be kept in mind. The arrangement is also very important in this examination.
Nursing Care of patient while giving enema. Enemas are injections of fluids used to cleanse or stimulate the emptying of your bowel. This procedure has been used for years to treat constipation and similar issues. Constipation is a severe condition that slows down the movement of your stool. It also makes the stool hard and difficult to excrete. # Study Purpose # For nursing students
General Physical Examination is an essential part of all the examinations of human body. a brief knowledge of every step of this examination must be kept in mind. The arrangement is also very important in this examination.
Nursing Care of patient while giving enema. Enemas are injections of fluids used to cleanse or stimulate the emptying of your bowel. This procedure has been used for years to treat constipation and similar issues. Constipation is a severe condition that slows down the movement of your stool. It also makes the stool hard and difficult to excrete. # Study Purpose # For nursing students
Retina (Define ,anatomy of retina, examination of retina, classification of ...Maryam Fida
Retina
The retina is a layer tissue at the back of the eye that senses light and sends images to the brain. In the center of this nervous tissue is the macula, that allows to focus the view toward the center and provides the needed sharpness to read, drive and clearly see details.
The retina processes light through a layer of photoreceptor cells. These are essentially light-sensitive cells, responsible for detecting qualities such as color and light-intensity. The retina processes the information gathered by the photoreceptor cells and sends this information to the brain via the optic nerve. Basically, the retina processes a picture from the focused light, and the brain is left to decide what the picture is.
Layers of Retina
The retina can be divided into 11 layers including
1. the inner limiting membrane
2. the nerve fiber layer
3. the ganglion cell layer
4. the inner plexiform layer
5. the inner nuclear layer
6. middle limiting layer
7. the outer plexiform layer
8. the outer nuclear layer
9. the outer limiting membrane
10. the photoreceptor layer
11. The retinal pigmented epithelium (RPE) monolayer.
Ora serrata
Anterior termination of retina where it continues with epithelium of Ciliary body.
Macula lutea (yellow spot)
1.5mm diameter area at post. Pole about 3mm temporal to optic disc.
Fovea centralis
Small depression in centre of macula
Cones predominate in this area
Most sensitive part of retina
Figure 1 Normal fundus Vessels emerge from nasal side of disc. Arteries are narrower than veins
Examination of Retina
Direct & indirect Ophthalmoscopy
1. Darken room, ask patient to look at the same point as far as possible in the room (this will help to dilate the pupil).
2. Wedge scope against your cheek with hand and then head/hand/scope should move as one unit.
3. Use your right hand & your right eye to look at the patient’s right eye. (Less important if using the PanOptic.)
4. Look through the ophthalmoscope, if you are nearsighted and have taken off your glasses, you may need to adjust the focusing wheel towards the negative/red until what you see at a distance is in focus.
5. Direct the ophthalmoscope 15 degrees from center and look for the red reflex (see video). Simply follow the red reflex in until you see the retina. If you lose the red reflex, come back until you find it again and repeat.
6. To look around the retina using a traditional direct ophthalmoscope, you should "pivot" the ophthalmoscope, angling up, down, left and right. If using the PanOptic, you can slightly "pivot" or ask the patient to look up to see upper retina, down to see lower retina, medial to see medial, latereral to see lateral and finally to look at the light to visualize the macula.
Slit Lamp Binocular Indirect Ophthalmoscopy
The use of slit lamp BIO is an increasingly popular form of fundoscopic examination. Minimum a dilated fundus examination with an indirect lens should be carried out on those presenting with photopsi
This pdf is about the Schizophrenia.
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Richard's entangled aventures in wonderlandRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
A brief information about the SCOP protein database used in bioinformatics.
The Structural Classification of Proteins (SCOP) database is a comprehensive and authoritative resource for the structural and evolutionary relationships of proteins. It provides a detailed and curated classification of protein structures, grouping them into families, superfamilies, and folds based on their structural and sequence similarities.
8. PUPILLARY REACTIONS
● Pupillary size changes in response
to light and to the effort of focusing
on a near object
LIGHT REACTIONS
● Direct Light reflex
● Consensual light reflex
11. When the person is looking downward to the right = Right Inferior rectus muscle (CN III)
Left
Superior Oblique muscle (CN IV)
If one of these muscles is paralyzed, the eye will deviate from its normal
position in that direction of gaze and the yes will no longer appear conjugate
or parallel
12. TECHNIQUES of EXAMINATION
Important Areas of Examination
● Visual Acuity
● Visual Fields
● Conjunctiva and sclera
● Cornea, lens, and pupils
● Extraocular Movements
● Fundi, including: Optic disc and cup, retina, and retinal vessels
13. 1. Visual Acuity
● Test the acuity of central vision using Snellen
eye chart
● Procedure:
1. Position the pt 20ft from the chart
2. Ask the pt to cover one eye with a card and
to read the smallest line of print possible
3. Identify the smallest line of print where the
patient can identify more than half the
letters
4. Record the visual acuity designated at the
side of this line.
14. 2. VISUAL FIELDS by CONFRONTATION
● For detection of lesions in the anterior and posterior visual pathway
○ Causes of anterior pathway defects include glaucoma, optic neuropathy, optic neuritis,
and glioma. Posterior pathway defects include stroke and chiasmal tumors
● Studies recommend combining two tests to achieve the best results : the
static finger wiggle test and the kinetic red target test
15. Static Finger Wiggle Test
Procedure:
1. Position yourself about an arm’s length away
from the pt
2. Close one eye and have the pt cover the
opposite eye while staring at your open eye
3. Place your hands about 2 ft apart out of pt’s
view, roughly lateral to the patient’s ears.
4. While in this position, wiggle your fingers and
slowly bring your moving fingers forward into
the pt’s center of view
5. Ask the pt to tell you as soon as he or she sees
your finger movt
16. Kinetic Red Target Test.
Procedure:
1. Facing the pt, move a 5mm red topped pin
inward beyond the boundary of each quadrant
along a line bisecting the horizontal and vertical
meridians
2. Ask the pt when the pin first appears to be red.
17. Position and Alignment of the Eyes
● Stand in front of the pt & survey the eyes for position & alignment. If one or both eyes
seem to protrude, assess them from the above.
Eyebrows
● Inspect eyebrows, noting their fullness, hair distribution, and any scaliness of the
underlying skin
Eyelids
● Note the position of the lids in relation to the eyeballs. Inspect for: width of the palpebral
fissures, edema of the lids, color of the lids, lesions condition & direction of of the eyelashes,
and adequacy of eyelid closure
Lacrimal Apparatus
● Briefly inspect the regions of the lacrimal gland and lacrimal sac for swelling
18. 3. CONJUNCTIVA and SCLERA
● Inspect the sclera & palpebral
conjunctiva for color (A yellow
sclera indicates jaundice)
● Note the vascular pattern against
the white scleral background.
● Look for nodules or swelling.
● If you need a fuller view of the
eye, rest your thumb & finger on
the bones of the cheek and
brow, & spread the lids.
19. 4. CORNEA, LENS, IRIS, and PUPILS
Cornea and Lens. With oblique lighting, inspect the cornea for opacities. Note any
opacities in the lens that maybe visible through the pupil
Iris. The markings should be clearly defined. With light shining directly from the
temporal side, look for crescentic shadow on the medial side of the iris. Because the iris
is normally fairly flat & forms a relatively open angle with the cornea, this lighting casts
no shadow.
20. Pupils. In a dim light, inspect the size, shape, and symmetry of both pupils. Measure the
pupils with card showing black circles of varying sizes, shown below & test the light
reaction. Note if the pupils are large (>5mm), small (<3mm), or unequal.
21. The Light Reaction
Ask the pt to look into the distance, & shine a bright light obliquely into each
pupil in turn.
Both the distant gaze and the oblique lighting help to prevent a near reaction.
Look for:
● Direct reaction (pupillary constriction in the same eye)
● Consensual reaction (pupillary constriction in the opposite eye)
Always darken the room & use bright light before deciding that a light reaction
is abnormal or absent
22. The Near Reaction
If the reaction to light is impaired or questionable, test the near reaction in both
dim & normal light.
● Hold your finger or pencil about 10cm from the pt’s eye.
● Ask the pt to look alternately at it and into the distance directly behind it.
● Watch for pupillary constriction with near effort & convergence of the
eyes.
23. Extraocular Muscles
•Standing about 2 feet directly in front of the patient, shine a
light into the patient’s eyes and ask the patient to look at it.
Inspect the light reflection in the corneas. They should be
visible slightly nasal to the center of the pupils.
28. Light Settings
● Large aperture is used for a dilated pupil after administering mydriatic
drops.
● Medium aperture is the standard for a non-dilated pupil in a dark room.
● Small aperture is for a constricted pupil in a well-lit room.
Ophthalmoscopic Examination
29. Ophthalmoscopic Examination
● Red free-used to look closely at the vasculature.
● Blue- Used to look for corneal abrasions or ulcers with fluorescein dye.
● Slit- Used to look at contour abnormalities of the cornea, lens or retina.
● Grid- Used to approximate the relative distance between retinal lesions.
30. Ophthalmoscopic Examination
● Wash your hands.
● Introduce yourself to the patient and explain what you are going to do.
● Position the patient so that the ophthalmoscope is held directly at the
level of the patient’s eye.
● Turn on the ophthalmoscope and set the light to the correct aperture.
● Dim the lights.
● Instruct the patient to focus on an object straight ahead on the wall.
● To exam the patient’s RIGHT eye, hold the ophthalmoscope in your RIGHT
hand and use your RIGHT eye to look through the instrument.
31. Ophthalmoscopic Examination
● Place your left hand on the patient’s head and place your thumb on
their eyebrow.
● Place yourself about 15 inches away from the patient and at an angle
15° lateral to the patient’s line of vision. Shine the light beam on the
pupil and look for the orange glow in the pupil—the red reflex.
32. Ophthalmoscopic Examination
● Now place the thumb of your other hand across the patient’s eyebrow,
which steadies your examining hand. Keeping the light beam focused on
the red reflex, move in with the ophthalmoscope on the 15° angle toward
the pupil until you are very close to it, almost touching the patient’s
eyelashes and the thumb of your other hand.
- Try to keep both eyes open and relaxed, as if gazing into the distance, to help
minimize any fluctuating blurriness as your eyes attempt to accommodate. -
You may need to lower the brightness of the light beam to make the
examination more comfortable for the patient, avoid hippus (spasm of the
pupil), and improve your observations.
33. Steps for Examining the Optic Disc and the Retina
❖ The optic disc is a round,
yellow-orange to creamy pink
structure with a pink
neuroretinal rim and central
depression that often takes
practice to locate. The
ophthalmoscope magnifies
the normal disc and retina
about 15 times and the
normal iris about 4 times. The
optic disc actually measures
about 1.5 mm.
34. Steps for Examining the Optic Disc
● First, locate the optic disc. Look for the round yellowish-orange structure
follow a blood vessel centrally until it enters the disc. The vessel size will
help you. The vessel size becomes progressively larger at each branch
point as you approach the disc.
35. Steps for Examining the Optic Disc
● Now, bring the optic disc into sharp focus by adjusting the lens of your
ophthalmoscope. If both you and the patient have no refractive errors,
the retina should be in focus at 0 diopters.
● If structures are blurred, rotate the lens disc until you find the sharpest
focus.
○ if the patient is myopic (nearsighted), rotate the lens disc counterclockwise to
the minus diopters.
○ in a hyperopic (farsighted) patient, move the disc clockwise to the plus
diopters.
36. Steps for Examining the Optic Disc
Inspect the optic disc. Note the following features:
● The sharpness or clarity of the disc outline. The nasal portion of the
disc margin may be somewhat blurred, a normal finding.
● The color of the disc, normally yellowish orange to creamy pink. White or
pigmented crescents may ring the disc, a normal finding.
● The size of the central physiologic cup, if present. It is usually yellowish
white. The horizontal diameter is usually less than half the horizontal
diameter of the disc.
● The comparative symmetry of the eyes and findings in the fundi.
37. Steps for Examining the Retina
● Inspect the retina, including arteries and veins as they extend to the
periphery, arteriovenous crossings, the fovea, and the macula. Distinguish
arteries from veins based on the features listed below.
Arteries Veins
Color Light red Dark red
Sze Smaller (2/3 to 3/4 the
diameter of veins)
Larger
Light reflex Bright Inconspicuous or absent
38. Steps for Examining the Retina
● Follow the vessels peripherally in each direction, noting their relative sizes
and the character of the arteriovenous crossings.
● Identify any lesions of the surrounding retina and note their size, shape,
color, and distribution. Lesions of the retina can be measured in terms of
“disc diameters” from the optic disc.
39. Steps for Examining the Retina
● Inspect the fovea and surrounding
macula. Direct your light beam
laterally or ask the patient to look
directly into the light.
● Inspect the anterior structures. Look
for opacities in the vitreous or lens.
Rotate the lens disc progressively to
diopters of around +10 or +12, so you
can focus on the more anterior
structures in the eye.
40. OPACITIES OF THE CORNEA AND LENS
Corneal/lens opacity is a disorder where in there is a transparent structure in front of the eyeball. This occurs when the cornea becomes scarred. Thus,
stops the light from passing through the cornea to the retina thereby causing the cornea appear white or cloudy in appearance
A. CORNEAL ARCUS
-A thin grayish white arc or circle
not quite at the edge of the
cornea
- suggests possible
hyperlipoproteinemia in young
adults (African Americans)
-this occurs because the lipids
forms around the iris because
of excessive levels of fat in
blood
41. OPACITIES OF THE CORNEA AND LENS
B. KAYSER-FLEISCHER RING
-A golden to red brown ring, sometimes
shading to green or blue, from copper
deposition in the periphery of the cornea
-Found in Wilson Disease
-rare autosomal recessive mutation of
the ATO7B gene on chromosome 13
causing abnormal copper
transport,(ceruloplasmin) reduced biliary
copper excretion, and abnormal
accumulation of copper in the liver and
tissues throughout the body.
42. OPACITIES OF THE CORNEA AND LENS
C. CORNEAL SCAR
-A superficial grayish white opacity
in the cornea, secondary to an old
injury or to inflammation
- Do not confuse with the opaque
lens of a cataract, visible on a
deeper plane and only through the
pupil
43. OPACITIES OF THE CORNEA AND LENS
D. PTERYGIUM
- A triangular thickening of the bulbar
conjunctiva that grows slowly across
the outer surface of the cornea,
usually from the nasal side
-Reddening may occur. May interfere
with vision as it encroaches on the
pupil
44. OPACITIES OF THE CORNEA AND LENS
E. CATARACTS
-Opacitiy of the lenses visible
through the pupil. Risk factors are
older age, smoking, diabetes,
corticosteroid use.
Nuclear cataracts: looks gray when
seen by a flashlight. If the pupil is
widely dilated, the gray opacity is
surrounded by a black rim.
45. OPACITIES OF THE CORNEA AND LENS
F. PERIPHERAL CATARACT
- Produces spokelike shadows that
point— gray against black, as seen
with a flashlight, or black against red
with an ophthalmoscope
46. PUPILLARY ABNORMALITES
A. UNEQUAL PUPILS (ANISOCORIA)- The light reaction in bright and dim light identifies the
abnormal pupil.
Constriction to light and near effort is mediated by parasympathetic pathways, and
pupillary dilatation by sympathetic pathways
When anisocoria is greater in bright light than in dim light, the larger pupil cannot constrict
properly
-causes: blunt trauma to the eye, open-angle glaucoma and impaired parasympathetic
innervation to the iris, as in tonic pupil and oculomotor nerve (CN III) paralysis.
When anisocoria is greater in dim light, the smaller pupil cannot dilate properly
- as in Horner syndrome, caused by an interruption of the sympathetic innervation.
48. A. UNEQUAL PUPILS (ANISOCORIA)
Tonic Pupil (Adie Pupil)
-affects the pupil of the eye and ANS
-the pupil of the affected eye is larger than the
unaffected eye and usually unilateral
-the affected pupil constricts SLOWLY (tonic) when
exposed to bright light
-These changes reflect parasympathetic
denervation.
- Slow accommodation causes blurred vision
- There is the abnormality to focus from distant to
near objects and vise versa
49. A. UNEQUAL PUPILS (ANISOCORIA)
● Oculomotor Nerve (CN III)
Paralysis
-The pupil is large and fixed to
light and near effort. Ptosis of
the upper eyelid(due to
impaired CN III innervation of
the levator palpebrae muscle)
and lateral deviation of the
eye downward and outward
are almost always present.
50. A. UNEQUAL PUPILS (ANISOCORIA)
Horner Syndrome
-The affected pupil is small, unilateral, reacts briskly to light and near effort, but dilates slowly, especially in dim light
These findings reflect the classic triad of Horner syndrome—miosis, ptosis and anhydrosis
due to a lesion in the sympathetic pathways anywhere
from the hypothalamus through the brachial plexus and cervical ganglia into the oculasympathetic fibers of the eye.
Causes include:
ipsilateral brainstem lesions, neck and chest tumors affecting the ipsilateral sympathetic ganglia and orbital trauma or
migraines
- In congenital Horner syndrome, the involved iris is lighter in color than its fellow (heterochromia).
52. A. UNEQUAL PUPILS (ANISOCORIA)
Small, Irregular Pupils (Argyll
Robertson Pupils)
- The pupils are small, irregular and
usually bilateral. They constrict with
near vision and dilate with far vision (a
normal near reaction) but do not react
to light, seen in neurosyphilis and rarely
in diabetes
53. B. EQUAL PUPILS AND ONE BLIND EYE
-Unilateral blindness does not cause anisocoria as long as the sympathetic and
parasympathetic innervation to both irises is normal. A light directed into the seeing eye
produces a direct reaction in that eye and a consensual reaction in the blind eye. A light
directed into the blind eye, however, causes no response in either eye. Normally, light
that is directed in one eye produces constriction in both eyes.
54. DYSCONJUGATE GAZE
A. Developmental Disorders-caused by an imbalance in ocular muscle
tone
Esotropia- form of strabisbus that is characterize by an inward turn of
one or both eyes while exotropia palabas or the outward eye turn
57. DYSCONJUGATE GAZE
B. Disorders of Cranial Nerves- New onset of dysconjugate gaze in adults
usually results from cranial nerve injuries, lesions, or abnormalities from
causes such as trauma, multiple sclerosis, syphilis, and others
59. NORMAL VARIATIONS OF OPTIC DISC
● PHYSIOLOGIC CUP - small whitish depression in the optic disc. Grayish
spots are often seen at its base.
the entry point for the retinal vessels. Although sometimes absent, the cup is
usually visible either centrally or toward the temporal side of the disc
60. NORMAL VARIATIONS OF OPTIC DISC
RINGS AND CRESCENTS- often seen around the optic disc. These are
developmental variations that appear as either white sclera, black retinal
pigment, or both, especially along the temporal border of the disc
61. NORMAL VARIATIONS OF OPTIC DISC
Medullated Nerve Fibers- Appearing as irregular white patches with
feathered margins, they obscure the disc edge and retinal vessels. They have
no pathologic significance
64. Special Techniques
Eye Protrusion (Proptosis or Exophthalmos)
● Stand behind the seated patient and inspect from above.
● Draw the upper lids gently upward, then compare the protrusion of the
eyes and the relationship of the corneas to the lower lids.
● Exophthalmometer: measures the distance between the lateral angle of
the orbit and an imaginary line across the most anterior point of the
cornea
● Upper limits of normal: 20 to 22 mm
● When protrusion exceeds normal, further evaluation by ultrasound or
computerized tomography scan often follows.
65. Special Techniques
Nasolacrimal Duct Obstruction
● Ask the patient to look up.
● Press on the lower lid close to the medial canthus, just inside the rim of
the bony orbit; this compresses the lacrimal sac.
● Look for fluid regurgitated out of the puncta into the eye.
● Avoid this test if the area is inflamed and tender.
66. Special Techniques
Everting the Upper Eyelid to Search for a Foreign Body
● Ask the patient to look down and relax the eyes. Be reassuring and use
gentle deliberate movements. Raise the upper eyelid slightly so that the
lashes protrude, then grasp the upper eyelashes and pull them gently
down and forward.
67. Special Techniques
Everting the Upper Eyelid to Search for a Foreign Body
● Place a small stick such as a tongue blade or an applicator at least 1 cm
above the lid margin at the upper border of the tarsal plate. Push down
on the tongue blade as you raise the edge of the lid, thus everting the
eyelid or turning it “inside out.” Do not press on the eyeball itself.
68. Special Techniques
Everting the Upper Eyelid to Search for a Foreign Body
● Secure the upper lashes against the eyebrow with your thumb and
inspect the palpebral conjunctiva. After your inspection, grasp the upper
eyelashes and pull them gently forward. Ask the patient to look up. The
eyelid will return to its normal position.
69. Special Techniques
Swinging Flashlight Test
● Clinical test for functional impairment of the optic nerves
● In dim light, note the size of the pupils.
● After asking the patient to gaze into the distance, swing the beam of a
penlight for 1 to 2 seconds first into one pupil, then into the other.
● Normally, each illuminated eye constricts promptly. The opposite eye also
constricts consensually.
77. Red Spots and Streaks in the Fundi
Superficial Retinal Hemorrhages—Small, linear, flame-shaped, red streaks in the fundi, shaped by the superficial
bundles of nerve fibers that radiate from the optic disc. Sometimes the hemorrhages occur in clusters and look like a
larger hemorrhage but can be identified by the linear streaking at the edges. These hemorrhages are seen in severe
hypertension, papilledema, and occlusion of the retinal vein, among other conditions. An occasional superficial
hemorrhage has a white center consisting of fibrin. White-centered retinal hemorrhages have many causes.
78. Preretinal Hemorrhage—Develops when blood escapes into the potential space between the retina and vitreous. This
hemorrhage is typically larger than retinal hemorrhages. Because it is anterior to the retina, it obscures any underlying
retinal vessels. In an erect patient, red cells settle, creating a horizontal line of demarcation between plasma above and
cells below. Causes include a sudden increase in intracranial pressure.
79. Deep Retinal Hemorrhages—Small, rounded, slightly irregular red spots that are sometimes called dot or blot
hemorrhages. They occur in a deeper layer of the retina than flame-shaped hemorrhages. Diabetes is a common cause.
80. Microaneurysms—Tiny, round, red spots commonly seen in and around the macular area. They are minute dilatations
of very small retinal vessels; the vascular connections are too small to be seen with an ophthalmoscope. A hallmark of
diabetic retinopathy.
81. Neovascularization—Refers to the formation of new blood vessels. They are more numerous, more tortuous, and
narrower than other blood vessels in the area and form disorderly looking red arcades. A common feature of the
proliferative stage of diabetic retinopathy. The vessels may grow into the vitreous, where retinal detachment or
hemorrhage may cause loss of vision.
Editor's Notes
Asymmetry of the corneal reflections indicates a deviation from normal ocular alignment. A temporal light reflection on one cornea, for example, indicates a nasal deviation of that eye.
Dysconjugate gaze: failure of the eyes to turn in the same direction.
Nystagmus: condition in which the eyes make repetitive, uncontrolled movements.
Pause the object in the lateral and upward gaze.
Lid lag: inability of the upper lid to follow the eye at the same velocity from up gaze to down gaze
Superior sclera is exposed
Ask the patient to follow your finger or pencil as you sweep through the six cardinal directions of gaze. Making a wide H in the air.
The test measures the distance from your eyes to where both eyes can focus without double vision
Half light: partially obstructed by a lens with cataract
Red free: hemorrhage (retina will be black and white)
Absence of a red reflex suggests an opacity of the lens (cataract) or, possibly, the vitreous (or even an artificial eye). Less commonly, a detached retina or, in children, a retinoblastoma may obscure this reflex.
In a refractive error, light rays from a distance do not focus on the retina.
In myopia, they focus anterior to the retina, in hyperopia, posterior to it.
Retinal structures in a myopic eye look larger than normal.
An enlarged cup suggests chronic open-angle glaucoma.
For eyes with exophthalmos, or unusual forward protrusion, stand...
Ophthalmologists use an exophthalmometer, which…
Exophthalmos is present in approximately 60% of patients with Graves ophthalmopathy and half of patients with Graves disease from autoimmune hyperthyroidism.
Common symptoms of Graves ophthalmopathy are diplopia and tearing, grittiness, and pain from corneal exposure.
Eyelid retraction (91%), extraocular muscle dysfunction (43%), ocular pain (30%), and lacrimation (23%) are also common.
This test helps identify the cause of excessive tearing.
As shown in the picture
Discharge of mucopurulent fluid from the puncta suggests an obstructed nasolacrimal duct.
To search thoroughly for a foreign body in the eye, evert the upper lid following these steps:
A foreign body in the eye often involves dust, a speck of sand, a paint chip, an insect, or a dislodged eyelash trapped underneath the lid, causing patients to sense something in their eye.
Foreign bodies can be superficial, sticking to the eye surface or beneath the lid, or penetrating—usually a piece of metal that pierces the outer cornea or sclera.
This view allows you to see the upper palpebral conjunctiva and look for a foreign body that might be lodged there.
In left-sided optic nerve damage, the pupils usually react as shown in the pictures:
When the light beam shines into the normal right eye, there is brisk constriction of both pupils (direct response on the right and consensual response on the left).
When the light swings over to the abnormal left eye, partial dilation of both pupils will occur. The afferent stimulus on the left is reduced, so the efferent signals to both pupils are also reduced and a net dilation occurs. This demonstrates an afferent pupillary defect, sometimes termed a Marcus Gunn pupil.
These are the tables lifted from the book of Bates…
From this table, we can see the comparisons between conjunctivitis, subconjunctival hemorrhage, corneal injury or infection, acute iritis, and acute angle closure glaucoma in terms of their pattern of redness, pain, vision, ocular discharge, pupil, cornea, and their clinical significance.
This table shows the different visual field defects...
This table shows the variations and abnormalities of the eyelids...
This table shows the lumps and swellings in and around the eyes...