What could be the cause if cerebellar dysfunction is acute/abrupt?
CVA or brain lesion
What could be the cause if cerebellar dysfunction has rapid progression (hours to days)?
What could be the cause if cerebellar dysfunction has slower progression (weeks to months)?
What could be the cause if cerebellar dysfunction is chronic (months to years)?
Primary method of diagnosis of cerebellar issues
brain and brainstem MRI
What happens to the cerebrum and cerebellum with alcoholic ataxia?
starts to shrivel up
What is the most noticeable symptom of cerebellar dysfunction?
ataxia - poor muscle control that causes clumsy voluntary movements
S&S of alcoholic ataxia
characteristics of Korsakoff’s psychosis
characteristics of Wernicke’s Encephalitis
What causes Wernicke-Korsakoff syndrome?
chronic alcohol use that leads to thiamine (vitamin B1) deficiency
What is chiari malformation?
congenital condition in which structural abnormalities lead to herniation of cerebellum through foramen magnum, compression involved structures
Type 1,2,3 of chiari malformation
Type 1 - symptoms appear in adolescence or adulthood
Type 2 - symptoms appear in childhood
Type 3 - symptoms appear in babies - rare but most severe
symptoms of chiari malformation
Can be asymptomatic
What is Friedreich’s ataxia? When do symptoms onset?
S&S of cerebellar Friedreich’s ataxia
S&S of non-cerebellar Friedreich’s ataxia
prognosis of Friedreich’s ataxia. What is the most common cause of death?
treatment - symptom management and functional training
What is spinocerebellar ataxia? What type of symptoms will be seen?
What is unique about spinocerebellar ataxia?
Significant degree of variations of presentation, prognosis, and progression because there are over 50 types
When does onset occur with spinocerebellar ataxia?
anywhere between childhood and adulthood
What will be seen with type 1 spinocerebellar ataxia?
most common
- optic atrophy
- ophthalmoplegia
- dementia/cog deficits
- amyotrophy - asymmetric lower limb motor neuropathy
- extrapyramidal signs
What are extrapyramidal signs?
basal ganglia impairments
- involuntary muscle contractions
- tremors
- stiff muscles
- bradykinesia
- involuntary movements
What will be seen with type 2 spinocerebellar ataxia?
dominated by visual loss
- retinal degeneration which may be associated with ophthalmoplegia and extrapyramidal signs