Nervous system

Cards (61)

  • Alzheimer's
    • Neurodegenerative disorder
    • Progressive loss of cognitive function
    • Affects brain
  • Etiology of Alzheimer's
    • Neurochemical factors
    • Viral factors
    • Trauma
    • Genetic factors
  • Neurochemical factors in Alzheimer's
    • Deficiencies in neurotransmitters acetylcholine, somatostatin, substance P, and norepinephrine
  • Viral factors in Alzheimer's
    • Slow-growing CNS viruses
  • Genetic factors in Alzheimer's
    • APOE, APOE-e4
  • Familial Alzheimer's

    Occurs very rarely on people with alzheimer’s
  • Sporadic Alzheimer's
    Most common
  • Pathogenesis of Alzheimer's
    • Neurofibrillary tangles formed from fibrous proteins in neurons
    • Beta-amyloid plaques (protein deposits)
    • Abnormal protein concentration and new protein formation
    • Granulovacuolar degeneration of neurons
  • Signs and Symptoms of Alzheimer's
    • Insidious onset
    • Extend over 10-20 years
    • Behavioral changes (early)
    • Irritability, hostility, mood swings (early)
    • Gradual loss of memory, lack of concentration (early)
    • Impaired learning, poor judgment (early)
    • Decline of cognitive function, memory, language (late)
    • Change in food intake (late)
    • Inability to recognize family, lack of environmental awareness, incontinence, inability to function, Urinary incontinence (late)
  • Treatment of Alzheimer's
    • Current drugs can't alter progressive loss of brain cells
    • Cholinesterase inhibitors prevent breakdown of acetylcholine
    • Possible vaccine in clinical trials to stimulate immune system against beta-amyloid plaques
  • Amyotrophic Lateral Sclerosis (ALS)

    • Progressive neurodegenerative disorder
    • Affects nerve cells in brain and spinal cord
    • Cognitive function remains normal
  • Etiology of ALS
    • Gene mutation
    • Chemical imbalance with high glutamate levels
    • Accumulation of abnormal proteins
    • Autoimmune disorders
    • Precipitating factors like trauma, viral infection, physical exhaustion
  • Familial ALS
    Rare (5-10%)
  • Sporadic ALS
    Most common (90-95%)
  • Signs and Symptoms of ALS
    • Onset between 40-70 years old
    • Motor neurons gradually die, cannot produce or transport signals to muscles
    • Leads to weakness, paralysis, muscle atrophy in upper limbs
  • Treatment of ALS
    • Patients may require gastric feedings, tracheostomy and mechanical ventilation
  • Bell's Palsy

    • Most common facial nerve disorder
    • Mild weakness to total paralysis on one side of face
    • Considered benign, most patients recover
  • Etiology of Bell's Palsy
    • Inflammation or compression of facial nerve
    • Acute demyelination of nerves
    • Reactivation of herpes simplex virus (HSV-1) or herpes zoster virus (HZV)
    • Viral infections causing nerve inflammation and compression
  • Risk Factors for Bell's Palsy
    • Pregnant women in 3rd trimester
    • Early postpartum
    • Older adults
    • People with diabetes or hypothyroidism
  • Signs and Symptoms of Bell's Palsy
    • Facial droop and trouble making facial expressions
    • Drooling
  • Epilepsy
    Neurologic disorder with abnormal brain activity causing seizures
  • Etiology of Epilepsy
    • Genetic influences
    • Perinatal injuries
    • Metabolic abnormalities
    • Brain conditions
    • Infections
    • Traumatic brain injury
    • Ingestion of toxins
    • High fever in young child
  • Pathogenesis of Epilepsy
    • Seizures are paroxysmal events with abnormal electrical discharges in the brain
    • Status epilepticus can lead to severe hypoxia, acidosis, and brain damage
  • Signs and Symptoms of Epilepsy
    • Seizures can trigger convulsive movements, interruption of sensation, or alteration in level of consciousness
    • Affects people of all ages, races, and backgrounds
    • Absence seizures common in children
    • Does not usually affect intelligence
  • Diagnosis of Epilepsy
    EEG is used to confirm diagnosis and classify seizures
  • Treatment of Epilepsy
    • Drug therapy to reduce seizure frequency and prevent occurrence
    • Surgery for drug-resistant cases to remove localized epileptic area
  • Guillain-Barré Syndrome

    • Acute inflammatory demyelinating polyneuropathy
    • Autoimmune process following viral or bacterial infection
  • Pathogenesis of Guillain-Barré Syndrome

    • Rapidly progressing acute autoimmune processes leading to segmented demyelination of peripheral nerves
  • Epidemiology of Guillain-Barré Syndrome

    • Occurs equally in both sexes, usually between ages 30-50
  • Phases of Guillain-Barré Syndrome
    • Acute phase (1-3 weeks)
    • Plateau phase (several days to 2 weeks)
    • Recovery phase (4 months to 3 years)
  • Meningitis
    Inflammation of the meninges (membranes surrounding the brain and spinal cord)
  • Causes of Meningitis
    • Escherichia coli (neonates)
    • Haemophilus influenzae (young children)
    • Neisseria meningitidis (children/young adults)
    • Streptococcus pneumoniae (older adults)
  • Pathogenesis of Meningitis
    • Microorganisms reach the brain via blood, nearby tissue, or direct access
    • Infections spread rapidly through the meninges
    • Inflammatory response leads to increased intracranial pressure
  • Signs and Symptoms of Meningitis
    • Sudden onset
    • Severe headache, back pain, photophobia
    • Nuchal rigidity, Kernig sign, Brudzinski sign
    • Vomiting, irritability, lethargy, fever, chills with leukocytosis
    • Progression to stupor or seizures
  • Diagnosis of Meningitis
    Examination of cerebrospinal fluid to identify causative organism
  • Treatment of Meningitis
    • Aggressive antimicrobial therapy
    • Specific treatment for increased intracranial pressure and seizures
    • Glucocorticoids to reduce inflammation
    • Vaccines available for some types
  • Migraine
    Episodic neurological disorder characterized by headaches
  • Etiology of Migraine
    • May involve changes in blood flow to the brain, brain metabolism, vascular, hormonal, or neurotransmitter components
  • Types of Migraine
    • Migraine with aura (visual, sensory, or motor symptoms)
    • Migraine without aura (more common)
  • Diagnosis of Migraine
    Made from medical history and physical examination, EEG and imaging may be used to rule out other diagnoses