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Multiple Sclerosis
chronic autoimmune disease that affects the CNS. Involves the demyelination and subsequent degeneration of nerve fibers in the CNS.
Bradykinesia
slow movement
Parkinson's disease
associated with a tremor and slow movement thought to be related to a lack of dopamine.
Can ALS involve cognitive impairment.
Yes much later in the disease
typical signs of of hydrocephalus in neonates
irritability, enlarged head, and feeding difficulties.
Purpose of Glasgow scale
to assess level of consciousness in person with brain injury
CVA
Stroke
cause of communicating hydrocephalus
increased intracranial pressure because of excess CSF
vascular dementia
brain injury resulting from ischemia or hemorrhage.
most common artery involved with a CVA
common carotid artery
does MS follow a predictable pattern of progression in all patients?
no. MS usually fluctuates between remissions and exacerbations
risk factors for stroke
1. hypertension
2. smoking
3. history of coronary artery disease
4. diabetes
5. hypercholesterolemia
ALS
amyotrophic lateral sclerosis
what type of neuron is progressive degeneration occurring with ALS
upper and lower motor neurons
temporary treatment for Myasthenia Gravis
anticholinesterase
one sided paralysis
hemiplegia
quadriplegia
paralysis in all extremities
paraplegia
paralysis in lower extremities
symptoms of hydrocephalus
confusion, papilledoma,
communicating hydrocephalus
impaired reabsorption of CSF (hemorrhage, meningitis, congenital absence of arachnoid villi)
Non-communication hydrocephalus
blockage preventing CSF flow into the subarachnoid space due to lesions (tumor, hemorrhage) or malformations (Chiari, Dandy-Walker)
Congenital hydrocephalus
typically genetically caused and leads to malformations or other faulty development
Acquired hydrocephalus
consequence of some other disease process (infection -meningitis, tumor, head trauma, hemorrhage.)
purpose of CSF
provide buoyancy and protection to the brain.
location of CSF in cranium
in the subarachnoid space between the pia mater and the arachnoid mater
early signs of increased intracranial pressure in adults
1. increased blood pressure
2. altered heart rate
3. vomiting
4. decreased consciousness, papilledema
early signs of increased intracranial pressure in neonates
1. increased head circumference
2. enlargement of
3. sunset eyes
4. difficulty feeding
5. scalp vein distention
duration of transient ischemic attack
1-24 hours.
pathophysiology of transient ischemic attack
partial obstruction of a blood vessel in the brain. (Like Angina.)
aphasia
difficulty speaking and understanding
thrombotic stroke
blood clot (thrombus) within a cerebral artery causing obstruction. Can also be due to atherosclerosis.
embolic stroke
fatty plaque or blood clot (embolism) breaks away and flows to brain where it blocks an artery.
hemorrhagic stroke
break in blood vessel (aneurysm) in brain
is a patient with heart disease likelier to have a thrombotic, embolic or hemorrhagic stroke?
embolic as heart disease can often cause
some consequences of CVA on the temporal lobe
1. memory loss
2. receptive aphasia (difficulty understanding but communicate non-sensically)
3. hearing loss
functions of the frontal lobe
1. higher intellectual function
2. ipsilateral motor control
3. speech production
broca's area
motor speech
occipital lobe
1. vision
2. visual perception
deficits with patients with right hemispherical strokes
1. left sided motor deficits
2.
Functions of Temporal lobe
1. hearing
2. memory
3. speech perception
Functions of Brain stem
1. respiratory & cardiac regulation
2. level of awareness
3. reticular activiating system
4. includes midbrain, pons, medulla obloganta
Wernicke's area
auditory comprehension
modifiable risk factors for stroke
hypertension, hyperlipidemia, smoking, diabetes, atrial fibrilation, carotid disease, coagulation disorders, sickle cell disease, obesity, sedentary lifestyle, heavy alcohol use, cocaine use
non-modifiable risk factors for stroke
older age, female gender, African American race, heredity (genetics)
parietal lobe
primary somatic sensory area
Diencephalon
1. body temperature regulation
2.pituitary hormone control
3. autonomic nervous system responses
4.includes
function of cerebellum
coordination
forms of dementia that present with short term memory loss
1. alzheimers
2. vascular dementia
3. Lewy Body Dementia
4. Frontotemporal dementia
risk factors for alzheimers
1. age
2. inflammation
3. oxidative stress
Manifestations of alzheimers
early: short term memory loss, denial of memory loss, depression
late; personality changes, agitation and sleep disorders, reasoning deficit, delusions or hallucinations, dysphagia
risk factors for vascular dementia
hypertension, arrhythmias, hyperlipidemia, diabetes, smoking, peripheral vascular disease
prevalence of vascular dementia
20-25% of all dementia patients
manifestations of vascular dementia
confusion, agitation, unsteady gait,
risk factors for lewy body disease
parkinson's disease,
pathophysiology of lewy body disease
lack of dopamine (like parkinson's)
manifestations of lewy body disease
parkinson's symptoms (bradykinesia, tremor at res, akinesiat) fluctuation in sleep-wake cycles, hallucinations
risk factors for frontotemporal disease
family history
age of onset of frontotemporal disease
younger- around 40
famous person associated with ALS
Lou Gherig
body parts associated with lower neurons
all lower body parts beneath the neck
body parts associated with upper neurons
all body parts associated with cranial nerves
motor neuron disorders
1. parkinson's disease
2. myasthenia gravis
3. Multiple Sclerosis
4. amyotrophic lateral sclerosis
pathophysiology of myasthenia gravis
chronic autoimmune disease. Antibodies destroying of post-synaptic acetylcholine receptors
pathophysiology of MS
Chronic autoimmune disease. increase in syncytin production which attacks myelin producing cells.
pathophysiology of parkinson's disease
loss of dopamine in basal ganglia
manifestations in parkinson's disease
tremor at rest, bradykinesia, akinesia, rigidity, mask like appearance, shuffling gait
manifestations of MS
loss of balance, present at younger ages, periods of remission and exacerbations
most common cause of death for patients with ALS
respiratory collapse
pathophysiology of ALS
unknown degenerative motor neuron (upper and lower) death; SODI gene
Manifestations of ALS
typically not a cognitive problem, slow progressive ascending weakness/paralysis, spasticity, dysphagia and respiratory complications.
manifestations of myasthenia gravis
skeletal muscle weakness, diplopia and ptosis, facial droop, dysphagia and respiratory complications
difference between myasthenia gravis and MS
MS have much more peripheral symptoms and you can recover from myasthenia gravis while with MS you can't