Week 8 BG Disorders and Diff Dx From PD Flashcards
what is normal pressure hydrocephalus (NPH)
older adults, 60+, slowly developing, slow enlargement of ventricles and reversible. Gait disturbances, urinary incontinence, dementia/cognition decline
What are some Parkinson’s plus syndromes and what are some characteristics
- progressive supra nuclear palsy (PSP)
- Multiple system atrophy
- don’t usually respond L-dopa (which is something that people with PD respond to).
what is progressive supra nuclear palsy (PSP)
bradykinesia, unstable gait with frequent falls, rigidity, vertical gaze palsy, cognitive impairments and more rapid progression
what is multiple system atrophy (MSA)
degeneration affecting the cortex and cerebellum as well as the BG that leads to
bradykinesia, rigidity, wide BOS, frontal lobe dysfunction, ANS dysfunction, shy-draper syndrome, striatonigral Degeneration and olivopontocerebellar atrophy
how can we differentiate MSA with PD
MSA has a wide BOS, and usually, in PD you have a small BOS
what is HD
huntington’s: generation of the BG, autosomal dominant trait, affecting 6.5/100,000
progressive, manifests by 30 years old and die within 15-25 years.
what are the motor HD symptoms
jerky movements, chorea, gait similar to PD, decreased cadence and wide BOS, postural issues like PD
what are the cognitive and behavioral symptoms of HD
dementia, memory loss, impaired judgement, personality changes.
HD prognosis
early signs of clumsiness, incoordination and jerkiness, and dementia and psychological dysfunction follows, then completely bed bound.