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Nsc Exam Questions And Answers

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NSC EXAM QUESTIONS AND ANSWERS What is Huntington's Disease? - ANSWER️inherited disorder, malfunction of Huntington gene located on chromosome 4 - repeat of CAG triplets What is the pathology of HD? - ANSWER️severe loss of neurons in the caudate and putamen with subsequent astrocytosis; head of caudate becomes shrunken and there is dilatation of the anterior horns of lateral ventricles; also see neuronal degeneration within the temporal and frontal lobes of the cerebral cortex, globus pallidus, thalamus, subthalamic nucleus, substantial nigra, and cerebellum What age does progressive supra nuclear palsy onset? - ANSWER️50s-60s What are the clinical features of progressive supra nuclear palsy that distinguish it from idiopathic PD? - ANSWER️truncal rigidity limb, tremor is rare, prominent early postural instability and falls, limitation of vertical gaze esp. downgaze What is very common in multiple system atrophy? - ANSWER️orthostatic hypotension What are the clinical features of multiple system atrophy? - ANSWER️Autonomic failure, OH, bradykinesia, asymmetrical tremor, rigidity, postural instability, cerebellar dysfunction, gait/limb ataxia, sustained gaze-evoked nystagmus What are the two subdivisions of MSA? - ANSWER️predominant parkinsonian symptoms, predominant cerebellar symptoms What is corticobasalganglionic degeneration? - ANSWER️Cortical atrophy of the frontal and parietal lobes and loss of dopamine in the substantia nigra What are the clinical features of corticobasalganglionic degeneration? - ANSWER️progressive dementia; limb apraxia in one arm (alien arm), rigidity, bradykinesia, no tremor, dystonia, visual or tactile spatial neglect, nonfluent aphasia, impaired eye movements in horizontal and up gaze What is Cri du Chat syndrome? - ANSWER️Chromosome 5 error What is the primary clinical feature of cri du chat? - ANSWER️hypotonia (which may evolve into hypertonia) What are the clinical features of a child infected with cytomegalovirus? - ANSWER️CP, microcephaly, seizures What are the clinical features of FAS? - ANSWER️fine motor deficits, visual motor deficits, balance deficits What is Fragile X syndrome? - ANSWER️X chromosome mutation, most common cause of ID What are the clinical features of Fragile X? - ANSWER️coordination and motor planning issues, seizures What is Hurler syndrome? - ANSWER️an autosomal recessive, lysosomal storage disorder What are the features of Hurler syndrome? - ANSWER️hydrocephalus What is Lesch-Nyhan syndrome? - ANSWER️an x-chromosome syndrome What are the clinical features of Lewy Body Dementia? - ANSWER️early presentation of cog sx with cog fluctuations, hallucinations, bradykinesia, rigidity, neuroleptic sensitivity, lack of motor asymmetry at onset Where is the lesion for PD: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER️substantia nigra Where is the lesion for Lewy Body Dementia: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER️basal ganglia + cortex Where is the lesion for corticobasalganglionic degeneration: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER️basal ganglia + cortex Where is the lesion for Multiple System Atrophy: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER️basal ganglia + cerebellum + brainstem Where is the lesion for Progressive Supranuclear Palsy: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER️brainstem How is each item on the UPDRS scored? - ANSWER️0 = normal, 4 = severe so a higher score is worse What are some PT interventions for clients with PD? - ANSWER️motor learning cueing (auditory and visual) mental rehearsal external focus of control dual-task training eccentric exercise What type of auditory cueing was the best for clients with PD? - ANSWER️when they gave themselves a cue out loud (such as "big steps"... "long strides Madruga") vs. having the therapist give the cue or trying to give themselves an internal/silent cue

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NSC EXAM QUESTIONS AND ANSWERS




What is Huntington's Disease? - ANSWER✔️inherited disorder, malfunction of Huntington gene
located on chromosome 4 - repeat of CAG triplets

What is the pathology of HD? - ANSWER✔️severe loss of neurons in the caudate and putamen
with subsequent astrocytosis; head of caudate becomes shrunken and there is dilatation of the
anterior horns of lateral ventricles; also see neuronal degeneration within the temporal and
frontal lobes of the cerebral cortex, globus pallidus, thalamus, subthalamic nucleus, substantial
nigra, and cerebellum

What age does progressive supra nuclear palsy onset? - ANSWER✔️50s-60s

What are the clinical features of progressive supra nuclear palsy that distinguish it from
idiopathic PD? - ANSWER✔️truncal rigidity > limb, tremor is rare, prominent early postural
instability and falls, limitation of vertical gaze esp. downgaze

What is very common in multiple system atrophy? - ANSWER✔️orthostatic hypotension

,What are the clinical features of multiple system atrophy? - ANSWER✔️Autonomic failure, OH,
bradykinesia, asymmetrical tremor, rigidity, postural instability, cerebellar dysfunction, gait/limb
ataxia, sustained gaze-evoked nystagmus

What are the two subdivisions of MSA? - ANSWER✔️predominant parkinsonian symptoms,
predominant cerebellar symptoms

What is corticobasalganglionic degeneration? - ANSWER✔️Cortical atrophy of the frontal and
parietal lobes and loss of dopamine in the substantia nigra

What are the clinical features of corticobasalganglionic degeneration? - ANSWER✔️progressive
dementia; limb apraxia in one arm (alien arm), rigidity, bradykinesia, no tremor, dystonia, visual
or tactile spatial neglect, nonfluent aphasia, impaired eye movements in horizontal and up gaze

What is Cri du Chat syndrome? - ANSWER✔️Chromosome 5 error

What is the primary clinical feature of cri du chat? - ANSWER✔️hypotonia (which may evolve
into hypertonia)

What are the clinical features of a child infected with cytomegalovirus? - ANSWER✔️CP,
microcephaly, seizures

What are the clinical features of FAS? - ANSWER✔️fine motor deficits, visual motor deficits,
balance deficits

What is Fragile X syndrome? - ANSWER✔️X chromosome mutation, most common cause of ID

What are the clinical features of Fragile X? - ANSWER✔️coordination and motor planning
issues, seizures

What is Hurler syndrome? - ANSWER✔️an autosomal recessive, lysosomal storage disorder

What are the features of Hurler syndrome? - ANSWER✔️hydrocephalus

What is Lesch-Nyhan syndrome? - ANSWER✔️an x-chromosome syndrome

What are the clinical features of Lewy Body Dementia? - ANSWER✔️early presentation of cog
sx with cog fluctuations, hallucinations, bradykinesia, rigidity, neuroleptic sensitivity, lack of
motor asymmetry at onset

Where is the lesion for PD: substantia nigra, basal ganglia + cortex, basal ganglia + cerebellum +
brainstem, brainstem? - ANSWER✔️substantia nigra

, Where is the lesion for Lewy Body Dementia: substantia nigra, basal ganglia + cortex, basal
ganglia + cerebellum + brainstem, brainstem? - ANSWER✔️basal ganglia + cortex

Where is the lesion for corticobasalganglionic degeneration: substantia nigra, basal ganglia +
cortex, basal ganglia + cerebellum + brainstem, brainstem? - ANSWER✔️basal ganglia + cortex

Where is the lesion for Multiple System Atrophy: substantia nigra, basal ganglia + cortex, basal
ganglia + cerebellum + brainstem, brainstem? - ANSWER✔️basal ganglia + cerebellum +
brainstem

Where is the lesion for Progressive Supranuclear Palsy: substantia nigra, basal ganglia + cortex,
basal ganglia + cerebellum + brainstem, brainstem? - ANSWER✔️brainstem

How is each item on the UPDRS scored? - ANSWER✔️0 = normal, 4 = severe so a higher score
is worse

What are some PT interventions for clients with PD? - ANSWER✔️motor learning

cueing (auditory and visual)

mental rehearsal

external focus of control

dual-task training

eccentric exercise

What type of auditory cueing was the best for clients with PD? - ANSWER✔️when they gave
themselves a cue out loud (such as "big steps"... "long strides Madruga") vs. having the therapist
give the cue or trying to give themselves an internal/silent cue

What activities is there good evidence for treating PD? - ANSWER✔️pace-controlled treadmill
training at a speed 10% greater than comfortable walking speed... the best evidence I think

dance

cycling

LSVT BIG

boxing

Tai Chi

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