Cms Other Neuro Ramos Association

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most common involuntary movement disorder

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essential tremor

Front 2

slowly progressive postural or kinetic tremor-predominanlty affects upper extremities

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essential tremor

Front 3

occurs with voluntary maintenance of position against gravity

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postural essential tremor

Front 4

occurs during voluntary movement

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kinetic essential tremor

Front 5

resolves during sleep

some voluntary control/suppression

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essential tremor

Front 6

normal reflexes and tone

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essential tremor

Front 7

drugs, drug withdrawal

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essential tremor

Front 8

inability to maintain normal posture and smoothness of movement

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cerebellar ataxia

Front 9

manifest either at birth or early life

non prog, intermittent, chronic/progress

cerebell atxa

Back 9

non prog

Front 10

cerebellar hypoplasia with or without other posterior fossa malformatioin, affecting the brainstem structures

non prog, intermittent, chronic/progress

cerebell atxa

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non prog

Front 11

hypotonia and development delays

ataxia recognized when unsuccessufl at independend walking

non prog, intermittent, chronic/progress

cerebell atxa

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non prog

Front 12

external stimuli often trigger symptoms or episodes

non prog, intermittent, chronic/progress

cerebell atxa

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intermittent

Front 13

many associated with molecular genetic abnormalities = identifiable biochemical defects

non prog, intermittent, chronic/progress

cerebell atxa

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chronic/progressive

Front 14

hypoactive knee and ankle deep tendon reflexes, babinski sign, impaired position sense

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friedreich ataxia

Front 15

hypertrophic cardiomyopathy

pes cavus, hammer toes

abnormal glucose tolreance test resuls

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friedreich ataxia

Front 16

malabsorptive state with steatorrhea and abdominal distension

pigmentary retinopathy

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abetalaproteinemia

Front 17

acanthocytosis on peripheral blood smears

constant finding

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abetalprotienemia

Front 18

year range for focal dystonia

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30-50

Front 19

sustained or repetive involuntary muscle contractions

frequently twisting movements with abnormal postures

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cerebellar atrophy

Front 20

intially elicated by voluntary movements action dystonia

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primary dystonia

Front 21

childhood onset

primaryl affects ashkenazi jews

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primary dystonia

Front 22

most common form of dystonia

30-50 years

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focal dystonia

Front 23

consequences of drus or other neurologic problems

which dystonia

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secondary dystonia

Front 24

progressive, fatal, autosomal dominant disorder characterized by motor, behavioral, and cognitive dysfunction

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huntingtoms chorea

Front 25

characterized by rapid, non pattered, semi purposeful

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huntingtons chorea

Front 26

dysarthra gait disturbace, and oculomotor abnormalities common features

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huntings chorea

Front 27

majority of huntings pts develop

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dementia

Front 28

brief, rapid, recurrent and seemingly purposeless stereoyped motor contraction

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tics

Front 29

movement only affecting individual muscle group

(blinking, twitching of nose, jerking of neck)

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simple tics

Front 30

coordinated involvment of multiple muscle groups

(jumping,sniffing, headbanging, echopraxia-mimikcking movements)

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complex tics

Front 31

may present in adulthood and or in associated withother disorders, including pd, hd, trauma, dystonia, drugs and toixins

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tics

Front 32

neurobehavioral disorder

characterized by multiple motor tics and vocalizations

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tourette syndrome

Front 33

most common form of facial parlysis

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bells palsy