Amyotrophic lateral sclerosis

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Amyotrophic lateral sclerosis

Neurologic system

Central nervous system disorders

Brain herniation
Broca aphasia
Kluver-Bucy syndrome
Wernicke aphasia
Acoustic neuroma (schwannoma)
Adult brain tumors
Adult brain tumors: Pathology review
Pediatric brain tumors
Pediatric brain tumors: Pathology review
Pituitary adenoma
Cerebral vascular disease: Pathology review
Ischemic stroke
Transient ischemic attack
Aqueductal stenosis
Cerebral palsy
Chiari malformation
Congenital neurological disorders: Pathology review
Dandy-Walker malformation
Septo-optic dysplasia
Spina bifida
Spinocerebellar ataxia (NORD)
Syringomyelia
Tethered spinal cord syndrome
Alzheimer disease
Creutzfeldt-Jakob disease
Dementia: Pathology review
Frontotemporal dementia
Lewy body dementia
Normal pressure hydrocephalus
Vascular dementia
Acute disseminated encephalomyelitis
Central pontine myelinolysis
Demyelinating disorders: Pathology review
JC virus (Progressive multifocal leukoencephalopathy)
Multiple sclerosis
Transverse myelitis
Cavernous sinus thrombosis
Cluster headache
Headaches: Pathology review
Idiopathic intracranial hypertension
Migraine
Tension headache
Trigeminal neuralgia
Brain abscess
Cavernous sinus thrombosis
Central nervous system infections: Pathology review
Creutzfeldt-Jakob disease
Encephalitis
Epidural abscess
Meningitis
Neonatal meningitis
Arteriovenous malformation
Epidural hematoma
Intracerebral hemorrhage
Saccular aneurysm
Subarachnoid hemorrhage
Subdural hematoma
Adrenoleukodystrophy (NORD)
Leukodystrophy
Essential tremor
Huntington disease
Movement disorders: Pathology review
Opsoclonus myoclonus syndrome (NORD)
Parkinson disease
Restless legs syndrome
Torticollis
Wernicke-Korsakoff syndrome
Peroxisomal disorders: Pathology review
Zellweger spectrum disorders (NORD)
Early infantile epileptic encephalopathy (NORD)
Epilepsy
Febrile seizure
Seizures: Pathology review
Brown-Sequard Syndrome
Cauda equina syndrome
Friedreich ataxia
Neurogenic bladder
Spinal cord disorders: Pathology review
Syringomyelia
Treponema pallidum (Syphilis)
Vitamin B12 deficiency
Concussion and traumatic brain injury
Shaken baby syndrome
Traumatic brain injury: Pathology review

Assessments

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High Yield Notes

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Flashcards

Amyotrophic lateral sclerosis

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Questions

USMLE® Step 1 style questions USMLE

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A 53-year-old male presents to his primary care physician with worsening hand and leg weakness. He often feels as if his left leg is “dragging” and experiences “spasms” while running. He additionally has difficulty holding a pen as firmly as he used to. Past medical history is notable for Graves disease. The patient does not smoke, use alcohol or other illicit substances. His temperature is 37.0°C (98.6°F), pulse is 65/min, respirations are 14/min, blood pressure is 125/64 mmHg, and O2 saturation is 98% on room air. Physical exam is notable for 4/5 strength in the right hand, with thenar muscle atrophy, as well as 4/5 strength in the left lower extremity. He has upgoing toes when the inner sole of the left foot is stroked. Which of the following best describes the pathophysiology of this disease? 

External References

First Aid

2024

2023

2022

2021

Amyotrophic lateral sclerosis (ALS)

spinal cord lesions p. 544

Summary

Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig's disease, is a neurodegenerative disease that affects both upper and lower motor neurons. Motor neurons reach from the brain to the spinal cord and from the spinal cord to muscles throughout the body. The progressive degeneration of these motor neurons leads to muscle weakness and atrophy.

ALS symptoms typically develop slowly over time. Early symptoms may include muscle weakness or stiffness, difficulty speaking, swallowing, or breathing. As the disease progresses, patients lose their ability to move and speak and eventually require total care. In some cases, people with ALS live for many years after diagnosis; however, most people with ALS die within a few years of diagnosis.