This document provides information to help localize neurological deficits based on symptoms and signs. It discusses localization in the upper motor neuron system including the cortex, corona radiata, internal capsule, brainstem, and spinal cord. It also discusses localization in the lower motor neuron system including the anterior horn, root/plexus, and nerves. Localization is guided by features like patterns of weakness, sensory loss, reflex changes, and specific cranial nerve involvement.
This document describes neurological signs and symptoms associated with different lesions in the central nervous system. It discusses upper and lower motor neuron syndromes, and provides details on localization of lesions in the brain, spinal cord, and specific areas like the medulla. Syndromes involving the middle cerebral artery, basilar artery, cranial nerves, and motor neuron disease are also outlined. The concluding sections cover inflammatory demyelinating polyneuropathy, neuromuscular junction disorders, and myopathies.
1. Hemiplegia is weakness on one side of the body that can be caused by stroke, brain tumors, infections, or head trauma.
2. Strokes are a common cause of hemiplegia and can be divided into thrombosis, embolism, or hemorrhage depending on the mechanism.
3. The location of the brain lesion determines the pattern of weakness and associated neurological signs, such as lesions in the internal capsule causing dense uniform weakness, or brainstem lesions potentially causing crossed hemiplegia.
This document discusses the clinical evaluation of hemiplegia. It provides details on brain anatomy, physiology, handedness and the contra-lateral control of the brain. It describes the blood supply of the brain including the Circle of Willis. The document examines the pathology of ischemic stroke and discusses assessing features such as the site of lesion localization, whether the deficit is ischemic or hemorrhagic in nature, and if it represents a transient ischemic attack, evolving stroke or completed stroke. Precise neurological examination is emphasized to determine the structures and tracts involved.
Monoplegia is paralysis of a single limb, usually an arm, which can be caused by cerebral palsy or affect just one muscle group. Paraplegia is impairment of motor and sensory function in the lower extremities, usually from spinal cord injury or conditions like spina bifida. Quadriplegia/tetraplegia is paralysis of all four limbs and the torso, resulting in loss of both sensation and motor control. Anesthesia temporarily blocks sensation including pain, allowing patients to undergo surgeries and procedures without distress. It is a pharmacologically induced reversible state of amnesia, loss of consciousness, and decreased stress response.
Paralysis is the complete loss of muscle function for one or more muscle groups and often includes loss of feeling in the affected area. It can be caused by damage to upper motor neurons, which convey signals from the brain to the nervous system, or lower motor neurons, which connect to muscles. Signs and symptoms depend on the location and severity of damage and may include numbness, tingling, pain, vision problems, speech difficulties, and breathing issues. Treatments focus on physical and occupational therapy to regain mobility, muscle strength, and independence through techniques like range of motion exercises and home modifications.
This document provides information to help localize neurological deficits based on symptoms and signs. It discusses localization in the upper motor neuron system including the cortex, corona radiata, internal capsule, brainstem, and spinal cord. It also discusses localization in the lower motor neuron system including the anterior horn, root/plexus, and nerves. Localization is guided by features like patterns of weakness, sensory loss, reflex changes, and specific cranial nerve involvement.
This document describes neurological signs and symptoms associated with different lesions in the central nervous system. It discusses upper and lower motor neuron syndromes, and provides details on localization of lesions in the brain, spinal cord, and specific areas like the medulla. Syndromes involving the middle cerebral artery, basilar artery, cranial nerves, and motor neuron disease are also outlined. The concluding sections cover inflammatory demyelinating polyneuropathy, neuromuscular junction disorders, and myopathies.
1. Hemiplegia is weakness on one side of the body that can be caused by stroke, brain tumors, infections, or head trauma.
2. Strokes are a common cause of hemiplegia and can be divided into thrombosis, embolism, or hemorrhage depending on the mechanism.
3. The location of the brain lesion determines the pattern of weakness and associated neurological signs, such as lesions in the internal capsule causing dense uniform weakness, or brainstem lesions potentially causing crossed hemiplegia.
This document discusses the clinical evaluation of hemiplegia. It provides details on brain anatomy, physiology, handedness and the contra-lateral control of the brain. It describes the blood supply of the brain including the Circle of Willis. The document examines the pathology of ischemic stroke and discusses assessing features such as the site of lesion localization, whether the deficit is ischemic or hemorrhagic in nature, and if it represents a transient ischemic attack, evolving stroke or completed stroke. Precise neurological examination is emphasized to determine the structures and tracts involved.
Monoplegia is paralysis of a single limb, usually an arm, which can be caused by cerebral palsy or affect just one muscle group. Paraplegia is impairment of motor and sensory function in the lower extremities, usually from spinal cord injury or conditions like spina bifida. Quadriplegia/tetraplegia is paralysis of all four limbs and the torso, resulting in loss of both sensation and motor control. Anesthesia temporarily blocks sensation including pain, allowing patients to undergo surgeries and procedures without distress. It is a pharmacologically induced reversible state of amnesia, loss of consciousness, and decreased stress response.
Paralysis is the complete loss of muscle function for one or more muscle groups and often includes loss of feeling in the affected area. It can be caused by damage to upper motor neurons, which convey signals from the brain to the nervous system, or lower motor neurons, which connect to muscles. Signs and symptoms depend on the location and severity of damage and may include numbness, tingling, pain, vision problems, speech difficulties, and breathing issues. Treatments focus on physical and occupational therapy to regain mobility, muscle strength, and independence through techniques like range of motion exercises and home modifications.
1) A comatose patient requires a thorough history, physical exam, and testing to identify the underlying cause. Important aspects of the exam include assessing ABCs, signs of trauma, meningeal irritation, pupil size/reactivity, eye and limb movements, and abnormal postures.
2) Brainstem lesions can be identified by evaluating pupillary size/reactivity, eye movements including nystagmus, oculocephalic reflex, and caloric response. Hemispheric lesions may cause hemiplegia.
3) The Glasgow Coma Scale is used to assess the level of consciousness on a scale of 3-15 based on the patient's motor response, verbal response, and eye opening
Ataxia is a syndrome of imbalance and incoordination involving gait, limbs, and speech that is caused by disorders of the cerebellum and/or its connections. The document discusses the clinical features, causes, diagnostic approach, and classification of different types of ataxia such as cerebellar ataxia, sensory ataxia, and psychogenic ataxia. Genetic causes of ataxia include autosomal recessive and dominant disorders as well as mitochondrial diseases.
[Int. med] motor symptoms from SIMS LahoreMuhammad Ahmad
This document discusses motor symptoms such as weakness, paresis, and increased fatigability. It describes upper and lower motor neuron lesions, providing signs of each. Upper motor neuron lesions can be caused by cerebrovascular accidents, tumors, or demyelination. Lower motor neuron lesions involve anterior horn cells or the peripheral nerve, neuromuscular junction, or muscles. Types of weakness like hemiparesis and paraparesis are explained. The evaluation and etiology of hemiparesis is covered, noting it can be caused by cortical, cranial nerve, or high cervical spine lesions. The exam of the motor system and investigations for hemiparesis are also summarized.
This document discusses the motor nervous system and motor paralysis from multiple levels including:
- The motor cortex and its connections to other brain areas
- The extrapyramidal and pyramidal systems
- Different types of apraxia and their lesion locations
- Lesions of the brainstem, spinal cord, nerves and muscles that can cause hemiplegia, monoplegia, or paraplegia
- The clinical features and localization of upper and lower motor neuron lesions
- Specific motor syndromes and their etiologies
It provides an overview of the organization of the motor system and localization of lesions throughout the nervous system that can result in different clinical motor deficits.
A seizure is a sudden, uncontrolled electrical disturbance in the brain. It can cause changes in your behavior, movements or feelings, and in levels of consciousness. If you have two or more seizures or a tendency to have recurrent seizures, you have epilepsy.
This document provides an overview of paraplegia in children, including definitions, causes, classifications, clinical features, investigations, associated conditions, management, and complications. Paraplegia is defined as impairment of motor function in the lower extremities, which can be caused by lesions in the brain, spinal cord, or peripheral nerves. Causes include infection, inflammation, tumors, trauma, vascular issues, and inherited or metabolic conditions. Management involves general care, physiotherapy, symptom treatment, and addressing the underlying cause. Complications can include bedsores, contractures, infections, and blood clots.
Epilepsy is a brain disorder caused by disturbed neuronal activity in the brain, which can cause strange sensations, emotions, behaviors, or sometimes convulsions. It is classified as either primary generalized or partial seizures. Diagnosis involves EEG, brain imaging, and blood tests to identify potential causes. Treatment primarily consists of anti-seizure medications, but may also include dietary therapies, vagus nerve stimulation, or surgery to remove the affected part of the brain.
This document summarizes the pathophysiology of seizures. It outlines predisposing factors like family history and precipitating factors like sensory stimuli. It then describes how an epileptogenic focus becomes hyperexcitable, leading to partial depolarization and neurotransmitter release. This lowers the seizure threshold and can be activated by precipitating factors, spreading abnormal electrical discharges between hemispheres. During the tonic phase, muscles stiffen and consciousness is lost. The clonic phase involves rapid muscle contractions and jerking. Finally, the post-ictal phase involves exhaustion and impaired coordination or consciousness.
Paraparesis, paraplegia, quadriparesis, and quadriplegia are sequelae of bilateral damage to the corticospinal tracts. Causes include spinal lesions such as spinal cord compression from tumors or diseases like multiple sclerosis, and cerebral lesions from conditions like cerebral palsy. Spinal cord compression is a medical emergency that requires early diagnosis and treatment to prevent permanent neuronal damage. Symptoms depend on the anatomical level and nature of the pathology, and may include pain, weakness, sensory changes, and urinary or bowel dysfunction. Magnetic resonance imaging is the primary diagnostic tool to localize and characterize lesions. Management involves treating any underlying condition causing compression, and rehabilitation to prevent complications and maximize functioning
The document provides guidance on performing a neurological examination to systematically evaluate patients for neurological abnormalities. It discusses evaluating the patient's conscious state, cognition, cranial nerves, motor system, sensory system, and extrapyramidal signs. The examination aims to detect any neurological abnormalities, localize them within the nervous system, and determine the specific lesion.
This document discusses seizure classification according to the International League Against Epilepsy in 2017. It defines a seizure as the clinical expression of abnormal neuronal activity in the brain, typically lasting seconds to minutes. Seizures are classified as focal onset, generalized onset, or unknown onset, with further subcategories of motor or non-motor seizures. Focal onset seizures may be subtle or unusual, while generalized onset include absence seizures, tonic-clonic, and myoclonic jerks. The document provides descriptions to help classify example seizure histories.
Cns case-extramedullary compressive myelopathy, Q&AKurian Joseph
Tracts involved-corticospinal tract
anterior and lat spinothalamic
posterior coloumn
Mostly extramedullary compressive myelopathy at T10 level
Etiology –to consider both intra and extradural causes like neurofibroma/meningioma/av malformation.
extradural-potts spine,ivdp
1) Stroke is defined as a sudden loss of brain function due to a disruption in blood flow to the brain. The two main types are ischemic (caused by blockage) and hemorrhagic (caused by bleeding).
2) Risk factors for stroke include hypertension, heart disease, diabetes, smoking, high cholesterol, previous TIA, family history, and age.
3) Ischemic strokes are caused by thrombosis or embolism and block blood vessels leading to "infarction" of brain tissue. Hemorrhagic strokes are caused by bleeding, usually from hypertension, aneurysms, or vascular malformations.
This document provides an overview of topics in applied neurosciences. It discusses the sensory system, special senses including the eye and ear, the motor system, cranial nerves, nerve conduction studies, EEG, neuro-microbiology, and several neurological disorders. Specific signs and symptoms of lesions in different areas of the nervous system are described. Various examination techniques for assessing the sensory and motor systems are also outlined.
This document provides an overview of cerebrovascular accidents (strokes) from a homeopathic perspective. It begins with definitions and classifications of strokes, including ischemic vs. hemorrhagic varieties. It then discusses risk factors, clinical classifications, and commonly indicated homeopathic remedies organized by mode of onset, anatomical site of lesions, and stage of disease. The remedies are proposed for preventing attacks, managing acute symptoms, and addressing remote changes. Overall, the document aims to enhance understanding and therapeutic application of homeopathic medicines for strokes through analytical organization of relevant clinical factors.
1. The document discusses the evaluation of a comatose patient, distinguishing between structural and metabolic causes of coma. 2. It describes assessing a patient's level of consciousness using the Glasgow Coma Scale and checking for signs of herniation. 3. The priority is to identify cases where progressive herniation may lead to further damage or death, and to separate metabolic from structural causes of coma.
The document discusses various states of consciousness including coma, stupor, and drowsiness. It describes potential causes of coma such as lesions in the reticular activating system or both cerebral hemispheres. Clinical signs that can help localize lesions are described, such as pupillary abnormalities suggesting brainstem involvement. The initial approach and assessment of a patient presenting with altered mental status or coma is outlined, including interventions, ancillary testing, and treatment in the emergency department. Various clinical signs are also described that may provide clues to the cause of coma.
This document provides an overview of epilepsy, including its history, epidemiology, classification, symptoms, investigation, treatment, and psychiatric complications. Some key points include:
- Epilepsy is a common neurological disorder affecting 20-40 million people worldwide.
- Seizures are classified as either generalized or partial based on where they originate in the brain. Common types include tonic-clonic, absence, myoclonic, and complex partial seizures.
- Investigations include EEG, MRI, and PET to help determine the seizure type and focus. Genetic factors are also important in some cases.
- Treatment involves anti-epileptic drugs to control seizures, with older drugs including phenytoin and
The document provides information on examining the nervous system. It discusses the components of the nervous system and how to examine different aspects including consciousness, cranial nerves, motor and sensory systems, coordination, and involuntary movements. The examination involves testing various functions like strength, reflexes, sensations, and gait to localize neurological deficits. Key signs help to differentiate upper and lower motor neuron lesions.
1) A comatose patient requires a thorough history, physical exam, and testing to identify the underlying cause. Important aspects of the exam include assessing ABCs, signs of trauma, meningeal irritation, pupil size/reactivity, eye and limb movements, and abnormal postures.
2) Brainstem lesions can be identified by evaluating pupillary size/reactivity, eye movements including nystagmus, oculocephalic reflex, and caloric response. Hemispheric lesions may cause hemiplegia.
3) The Glasgow Coma Scale is used to assess the level of consciousness on a scale of 3-15 based on the patient's motor response, verbal response, and eye opening
Ataxia is a syndrome of imbalance and incoordination involving gait, limbs, and speech that is caused by disorders of the cerebellum and/or its connections. The document discusses the clinical features, causes, diagnostic approach, and classification of different types of ataxia such as cerebellar ataxia, sensory ataxia, and psychogenic ataxia. Genetic causes of ataxia include autosomal recessive and dominant disorders as well as mitochondrial diseases.
[Int. med] motor symptoms from SIMS LahoreMuhammad Ahmad
This document discusses motor symptoms such as weakness, paresis, and increased fatigability. It describes upper and lower motor neuron lesions, providing signs of each. Upper motor neuron lesions can be caused by cerebrovascular accidents, tumors, or demyelination. Lower motor neuron lesions involve anterior horn cells or the peripheral nerve, neuromuscular junction, or muscles. Types of weakness like hemiparesis and paraparesis are explained. The evaluation and etiology of hemiparesis is covered, noting it can be caused by cortical, cranial nerve, or high cervical spine lesions. The exam of the motor system and investigations for hemiparesis are also summarized.
This document discusses the motor nervous system and motor paralysis from multiple levels including:
- The motor cortex and its connections to other brain areas
- The extrapyramidal and pyramidal systems
- Different types of apraxia and their lesion locations
- Lesions of the brainstem, spinal cord, nerves and muscles that can cause hemiplegia, monoplegia, or paraplegia
- The clinical features and localization of upper and lower motor neuron lesions
- Specific motor syndromes and their etiologies
It provides an overview of the organization of the motor system and localization of lesions throughout the nervous system that can result in different clinical motor deficits.
A seizure is a sudden, uncontrolled electrical disturbance in the brain. It can cause changes in your behavior, movements or feelings, and in levels of consciousness. If you have two or more seizures or a tendency to have recurrent seizures, you have epilepsy.
This document provides an overview of paraplegia in children, including definitions, causes, classifications, clinical features, investigations, associated conditions, management, and complications. Paraplegia is defined as impairment of motor function in the lower extremities, which can be caused by lesions in the brain, spinal cord, or peripheral nerves. Causes include infection, inflammation, tumors, trauma, vascular issues, and inherited or metabolic conditions. Management involves general care, physiotherapy, symptom treatment, and addressing the underlying cause. Complications can include bedsores, contractures, infections, and blood clots.
Epilepsy is a brain disorder caused by disturbed neuronal activity in the brain, which can cause strange sensations, emotions, behaviors, or sometimes convulsions. It is classified as either primary generalized or partial seizures. Diagnosis involves EEG, brain imaging, and blood tests to identify potential causes. Treatment primarily consists of anti-seizure medications, but may also include dietary therapies, vagus nerve stimulation, or surgery to remove the affected part of the brain.
This document summarizes the pathophysiology of seizures. It outlines predisposing factors like family history and precipitating factors like sensory stimuli. It then describes how an epileptogenic focus becomes hyperexcitable, leading to partial depolarization and neurotransmitter release. This lowers the seizure threshold and can be activated by precipitating factors, spreading abnormal electrical discharges between hemispheres. During the tonic phase, muscles stiffen and consciousness is lost. The clonic phase involves rapid muscle contractions and jerking. Finally, the post-ictal phase involves exhaustion and impaired coordination or consciousness.
Paraparesis, paraplegia, quadriparesis, and quadriplegia are sequelae of bilateral damage to the corticospinal tracts. Causes include spinal lesions such as spinal cord compression from tumors or diseases like multiple sclerosis, and cerebral lesions from conditions like cerebral palsy. Spinal cord compression is a medical emergency that requires early diagnosis and treatment to prevent permanent neuronal damage. Symptoms depend on the anatomical level and nature of the pathology, and may include pain, weakness, sensory changes, and urinary or bowel dysfunction. Magnetic resonance imaging is the primary diagnostic tool to localize and characterize lesions. Management involves treating any underlying condition causing compression, and rehabilitation to prevent complications and maximize functioning
The document provides guidance on performing a neurological examination to systematically evaluate patients for neurological abnormalities. It discusses evaluating the patient's conscious state, cognition, cranial nerves, motor system, sensory system, and extrapyramidal signs. The examination aims to detect any neurological abnormalities, localize them within the nervous system, and determine the specific lesion.
This document discusses seizure classification according to the International League Against Epilepsy in 2017. It defines a seizure as the clinical expression of abnormal neuronal activity in the brain, typically lasting seconds to minutes. Seizures are classified as focal onset, generalized onset, or unknown onset, with further subcategories of motor or non-motor seizures. Focal onset seizures may be subtle or unusual, while generalized onset include absence seizures, tonic-clonic, and myoclonic jerks. The document provides descriptions to help classify example seizure histories.
Cns case-extramedullary compressive myelopathy, Q&AKurian Joseph
Tracts involved-corticospinal tract
anterior and lat spinothalamic
posterior coloumn
Mostly extramedullary compressive myelopathy at T10 level
Etiology –to consider both intra and extradural causes like neurofibroma/meningioma/av malformation.
extradural-potts spine,ivdp
1) Stroke is defined as a sudden loss of brain function due to a disruption in blood flow to the brain. The two main types are ischemic (caused by blockage) and hemorrhagic (caused by bleeding).
2) Risk factors for stroke include hypertension, heart disease, diabetes, smoking, high cholesterol, previous TIA, family history, and age.
3) Ischemic strokes are caused by thrombosis or embolism and block blood vessels leading to "infarction" of brain tissue. Hemorrhagic strokes are caused by bleeding, usually from hypertension, aneurysms, or vascular malformations.
This document provides an overview of topics in applied neurosciences. It discusses the sensory system, special senses including the eye and ear, the motor system, cranial nerves, nerve conduction studies, EEG, neuro-microbiology, and several neurological disorders. Specific signs and symptoms of lesions in different areas of the nervous system are described. Various examination techniques for assessing the sensory and motor systems are also outlined.
This document provides an overview of cerebrovascular accidents (strokes) from a homeopathic perspective. It begins with definitions and classifications of strokes, including ischemic vs. hemorrhagic varieties. It then discusses risk factors, clinical classifications, and commonly indicated homeopathic remedies organized by mode of onset, anatomical site of lesions, and stage of disease. The remedies are proposed for preventing attacks, managing acute symptoms, and addressing remote changes. Overall, the document aims to enhance understanding and therapeutic application of homeopathic medicines for strokes through analytical organization of relevant clinical factors.
1. The document discusses the evaluation of a comatose patient, distinguishing between structural and metabolic causes of coma. 2. It describes assessing a patient's level of consciousness using the Glasgow Coma Scale and checking for signs of herniation. 3. The priority is to identify cases where progressive herniation may lead to further damage or death, and to separate metabolic from structural causes of coma.
The document discusses various states of consciousness including coma, stupor, and drowsiness. It describes potential causes of coma such as lesions in the reticular activating system or both cerebral hemispheres. Clinical signs that can help localize lesions are described, such as pupillary abnormalities suggesting brainstem involvement. The initial approach and assessment of a patient presenting with altered mental status or coma is outlined, including interventions, ancillary testing, and treatment in the emergency department. Various clinical signs are also described that may provide clues to the cause of coma.
This document provides an overview of epilepsy, including its history, epidemiology, classification, symptoms, investigation, treatment, and psychiatric complications. Some key points include:
- Epilepsy is a common neurological disorder affecting 20-40 million people worldwide.
- Seizures are classified as either generalized or partial based on where they originate in the brain. Common types include tonic-clonic, absence, myoclonic, and complex partial seizures.
- Investigations include EEG, MRI, and PET to help determine the seizure type and focus. Genetic factors are also important in some cases.
- Treatment involves anti-epileptic drugs to control seizures, with older drugs including phenytoin and
The document provides information on examining the nervous system. It discusses the components of the nervous system and how to examine different aspects including consciousness, cranial nerves, motor and sensory systems, coordination, and involuntary movements. The examination involves testing various functions like strength, reflexes, sensations, and gait to localize neurological deficits. Key signs help to differentiate upper and lower motor neuron lesions.
This document provides an overview of approaches to seizure and epilepsy diagnosis and classification. It discusses the differential diagnosis of seizures and conditions that can mimic seizures like syncope. It describes focal seizures which originate in one hemisphere and can involve motor, sensory or cognitive symptoms. Generalized seizures rapidly engage both hemispheres and include absence seizures, tonic-clonic seizures and atonic seizures. Seizures are classified based on their origin and symptoms. The EEG findings for different seizure types are also outlined.
Epilepsy is a common neurological disorders in which there will be an abnormal electrical activities in the brain causing a brief disruption in the communication system of the brain cells.
Epilepsy has a very common symptoms of seizures. A seizure is a sudden rise in electrical activity of the brain. It can involve a part of the brain or the entire brain.
To know more details --> https://www.icliniq.com/articles/neurological-health/what-exactly-is-epilepsy
The document provides information about strokes and cerebrovascular accidents. It defines different types of strokes including transient ischemic attack (TIA), reversible ischemic neurological deficit (RIND), and completed stroke. It discusses how to diagnose strokes by determining the neurological deficit, lesion location, type of lesion, and cause. The document also covers stroke risk factors, common locations for strokes including the middle cerebral artery (MCA), anatomy of the brain and blood supply, and types of strokes such as infarction and hemorrhage.
This document provides an overview of seizures and epilepsy, including:
1. It defines seizures and describes different seizure types such as partial seizures, absence seizures, tonic-clonic seizures, myoclonic seizures, and neonatal/infantile seizures.
2. Etiologies and classifications of epilepsy are discussed, including focal vs generalized and age-specific syndromes.
3. Details are given on symptoms, EEG findings, and treatment responses for different seizure types like partial motor/sensory seizures and complex partial seizures.
4. Causes of seizures including genetic, structural, metabolic and other factors are briefly outlined.
This document provides information on convulsions and epilepsy in children. It discusses the history of epilepsy, notable figures associated with epilepsy like St. Valentine, important epilepsy awareness days, common misconceptions about epilepsy, types of seizures including partial seizures, generalized seizures, absence seizures, and infantile spasms. It also covers the classification, causes, mechanisms, and syndromes of epilepsy as well as comparisons between different seizure types.
This document provides information on seizures and epilepsy. It defines seizures as abnormal excessive hypersynchronous discharges from the central nervous system. Seizures can be classified as partial or generalized. Partial seizures originate in a specific area of the brain and include simple partial and complex partial seizures. Generalized seizures involve both hemispheres and include absence seizures (petit mal), tonic-clonic seizures (grand mal), tonic, atonic, and myoclonic seizures. The document describes the clinical features and EEG patterns associated with different seizure types.
This document provides an overview of seizures and epilepsy. It defines seizures as clinical manifestations of abnormal neuronal electrical activity and epilepsy as two or more unprovoked seizures occurring more than 24 hours apart. Several seizure and epilepsy classifications are discussed. The pathophysiology of seizures is incompletely understood but may involve excitatory neurotransmitters and genetic factors. Diagnosis involves differentiating seizures from other events through history, exam, and tests like EEG.
This presentation is on comprehensive yet complete bedside neurological examination including higher mental functions, cranial nerve examinations, motor examination, sensory examination, cerebellar examination, extra pyramidal system examination.
- Seizures are caused by abnormal excessive neuronal activity in the brain and can be classified as either partial or generalized seizures. Partial seizures originate in a localized region of the brain while generalized seizures involve both hemispheres.
- Common types of generalized seizures include absence seizures, characterized by brief lapses of consciousness, and tonic-clonic seizures which involve tonic muscle contraction followed by clonic movements.
- Complex partial seizures originate in the temporal lobe and involve psychic experiences such as hallucinations followed by automatisms like lip smacking and confusion after the seizure.
This document summarizes information about convulsive disorders and epilepsy, including causes, types of seizures, classification, diagnosis, treatment, and prognosis. It discusses various types of seizures including partial, generalized tonic-clonic, absence, myoclonic, atonic, and febrile seizures. It also covers epilepsy syndromes, diagnostic testing including EEG and neuroimaging, differential diagnosis, management with antiepileptic drugs, and considerations in pregnancy. The majority of people with epilepsy experience remission within 10 years if their seizures are idiopathic and onset was in childhood.
The medulla oblongata is located in the brainstem and controls vital autonomic functions and reflexes such as breathing, heart rate, digestion and sneezing. It contains motor and sensory tracts that relay information between the brain and spinal cord. The medulla receives sensory information from the body and relays it to the cerebellum and thalamus. It also contains tracts that control voluntary movement and maintain posture. Injury to the medulla can cause paralysis, loss of sensation, difficulty swallowing and breathing problems and may result in death.
The document discusses various disorders of consciousness including changes in consciousness, focal neurological symptoms, causes, and first aid approaches. Key consciousness disorders covered include somnolence, sopor, coma, epilepsy, convulsive states, cerebrovascular accidents, meningitis, fainting, and conditions that can cause seizures such as febrile convulsions, eclampsia, tetany, tetanus, and botulinism. First aid focuses on ensuring safety, monitoring breathing and circulation, providing care specific to conditions like cooling for febrile seizures, and determining need for emergency medical treatment.
The document discusses epilepsy, which is a condition characterized by recurrent seizures. Seizures are classified as either partial or generalized. Partial seizures can be simple, complex, or lead to secondary generalization. Generalized seizures include absence, tonic-clonic, tonic, and myoclonic seizures. Causes of seizures include cerebral anoxia, infections, drugs, tumors, and metabolic disturbances. Management involves airway protection, benzodiazepines, and long-term antiepileptic drugs like carbamazepine, valproate, and phenytoin.
This document provides an overview of stroke including definitions, types, risk factors, signs and symptoms, assessments, and management. The key points are:
- Stroke is caused by interrupted blood flow to the brain and is classified as ischemic (caused by clot) or hemorrhagic (caused by bleeding).
- Risk factors include modifiable factors like hypertension, smoking, and diabetes as well as non-modifiable factors like age and heredity.
- Signs and symptoms vary depending on the affected brain region but may include weakness, sensory loss, vision issues, and speech problems.
- Assessments include imaging tests, neurological exam, and functional outcome measures to evaluate impair
The document provides guidance on approaching and managing a comatose patient. It outlines that the primary objectives are to stabilize, evaluate, and treat the patient by taking an organized sequential approach that prioritizes the airway, breathing, circulation, treating metabolic causes of coma like hypoglycemia, and evaluating for increased intracranial pressure or mass lesions. Secondary objectives include understanding the signs and symptoms of different causes of coma and developing a differential diagnosis. The document then provides detailed information on assessing different aspects of the comatose patient including their level of consciousness, neurological exam findings, breathing patterns, eye movements, motor response, and appropriate investigations.
Approach to a patient with CNS diseaseAhsan Sajjad
This document provides guidance on approaching and evaluating patients presenting with central nervous system disorders. It outlines the key presenting complaints to assess for and provides a framework for determining the location and etiology of any lesions. The approach involves a thorough history, physical exam focusing on neurological assessment, and selecting appropriate investigations. Common central nervous system disorders and patterns of deficits are discussed.
This document provides information about epilepsy including:
1. It defines epilepsy as two or more unprovoked seizures occurring more than 24 hours apart, with some exceptions. The incidence is about 3% globally.
2. It discusses the various causes/aetiologies of epilepsy including idiopathic, congenital, infections, trauma, vascular issues, tumors, and degenerative conditions.
3. It classifies seizure types according to the International League Against Epilepsy including partial seizures, generalized seizures like absence seizures, myoclonic seizures, and infantile spasms.
4. It outlines the management of epilepsy including establishing the diagnosis, deciding if antiepileptic drug therapy is
This document defines stroke as the sudden loss of neurological function caused by an interruption of blood flow to the brain. It classifies strokes as either ischemic, caused by a clot blocking blood flow, or hemorrhagic, caused by a ruptured blood vessel. Risk factors include hypertension, atrial fibrillation, and smoking. Symptoms vary depending on the affected brain region but may include weakness, sensory changes, speech problems, and visual issues. Complications can include muscle contractures, seizures, and cardiac or pulmonary issues.
Exocrine neoplasms of pancreas, Introduction: Fifth leading cause of deaths from cancer,
Aggressive tumor biology, Advanced stage of disease @ diagnosis, Lack of effective systemic therapies....
Beta lactam antibiotics & other cell wall synthesis inhibitorsDr. HIma
This document summarizes key information about penicillins and other beta-lactam antibiotics. It discusses their mechanisms of action inhibiting bacterial cell wall synthesis, pharmacokinetics varying by compound, clinical uses for treating various bacterial infections, and potential adverse effects like allergic reactions. Various subclasses are outlined including penicillins, cephalosporins, carbapenems, monobactams, and beta-lactamase inhibitor combinations. Specific antibiotics are highlighted along with their antimicrobial spectra and considerations for use.
Main and important classes of anti-hypertensive drugs.
(antihypertensive drugs, anti hypertensive sites of action, diuretics, diuretics sites of action, sympathoplegic drugs, beta blockers, alpha blokers, vasodilators, calcium channel blockers)
Iodine is essential for the production of thyroid hormones and is concentrated in glandular tissues like the thyroid, breasts, and salivary glands. It is absorbed from foods like iodized salt, seaweed, and fish, with the daily requirement being 150 mcg. Iodine deficiency can promote disorders like goiter and increase the risk of cancers. Iodine has many therapeutic actions including being antibacterial, antifungal, anticancer, and helping conditions like asthma, diabetes, and fibrocystic breast disease. It can be used as a diagnostic tool and to treat thyroid disorders as well as decreasing vascularity before thyroid surgery.
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Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
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These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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14. Absence/ petitmal
Brevity, frequency & paucity of motor activity
Absent mindedness, day dreaming
Sudden interuption of consciuosness
Patient stares, briefly stops responding
Minor automatisms – lip smacking, chewing,
fumbling movements of fingers
Remain motionless movements of eyelids,
facial muscles or fingers
Voluntary hyperventilation - triggers
15.
16.
17. Absence variants
2-2.5 spike wave
Atypical; Long runs of slow waves – can be
interrupted
Lennox gastaut syndrome – serious
1-2 slow wave
Intellectual impairment, minor tonic,clonic,
partial seizures
valproate
18. Myoclonic
Brief myoclonic jerks involving one part of
muscle – 50 – 100 ms
Associated with GTC, petit mal
Childhood – lafora type, myoclonus
-opsoclonus- ataxia
uremia
21. Frontal/ focal motor jacksonian
seizures
Supplementary motor area
Head and eyes turn opposite side – adversive,
area 6
Extension of limbs before loss of
consciousness due to expansion to thalamus,
mid brain RF
22. Jacksonian
Muscles of fingers, foot, arm, face
Premotor – 6, jacksonian
Fencing posture, 4,6,(8 choreathetotic,dystonic
); tonic extension and elevation of contralateral
arm
Todds paralysis
23. SOMATOSENSOR, visual
Numbness, tingling, pins and needles
Sylvian fissure – head
Superior sagital fissure – legs
Visual seizures – striate cortex, antero, occipito
temporal lobe
Darkness, flashes of light – opp eye
Auditary – buzzing or roaring – temporary lobe
Gustatory, vertigenous
24. Complex partial seizures
Adolscence, following febrile convulsions,
Secondary GTC
Focal seizure; temporal lobe – hallucinations,
alterd behaviour
Illusions – macro,micropsia, tilting of visual
environment, hallucinations,
dyscognitive states – strangeness to
environment, unfamiliar
Fear, anxiety
25.
Motor components – fumbling fingers,
chewing, lip smacking, daze walking,
unresponsiveness
Violence – temporal lobe
Gelastic epilepsy – no memory
Volvular – revolving in circles
Simple wndering aimless
No memory of aura, attack
Lesions in hippocampal,medial temporal
sclerosis
26.
Disoriented to time and place – right sided
lesion
Non – fluent aphasia
Nose wiping -temporal