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Results 1 - 10 of 13 for Cerebellar degeneration
  1. Boucher-Neuhäuser syndrome 
    ... P, Straumann D, Synofzik M. Boucher-Neuhauser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases ...
    https://medlineplus.gov/.../condition/boucher-neuhauser-syndrome - Genetics
  2. Microcephaly, seizures, and developmental delay 
    ... ataxia. It is unclear why some people have cerebellar nerve degeneration after birth in addition to impaired brain development ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  3. Primary coenzyme Q10 deficiency 
    ... the brain that is involved in coordinating movement (cerebellum). Other ... loss caused by degeneration (atrophy) of the optic nerves or breakdown of ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  4. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN) is a nervous system disorder with signs and symptoms that usually begin in mid-adulthood ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  5. Mainzer-Saldino syndrome 
    ... of scar tissue in the liver (hepatic fibrosis); cerebellar ataxia, which is difficulty with coordination and balance ... with a part of the brain called the cerebellum; and mild intellectual disability. Mainzer-Saldino syndrome is ...
    https://medlineplus.gov/genetics/condition/mainzer-saldino-syndrome - Genetics
  6. Spastic paraplegia type 15 
    ... cortex, which controls thinking and emotions, and the cerebellum, which coordinates movement.People with this form of ... impairs vision. This condition results from the breakdown (degeneration) of tissue at the back of the eye ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-15 - Genetics
  7. CLCN2-related leukoencephalopathy 
    ... condition. CC2L Leukoencephalopathy with ataxia Leukoencephalopathy with mild cerebellar ataxia and white matter edema Leukoencephalopathy with white ...
    https://medlineplus.gov/.../clcn2-related-leukoencephalopathy - Genetics
  8. Marinesco-Sjögren syndrome 
    ... Mutations in SIL1 cause Marinesco-Sjogren syndrome, a cerebellar ataxia with cataract and myopathy. Nat Genet. 2005 ...
    https://medlineplus.gov/.../condition/marinesco-sjogren-syndrome - Genetics
  9. CLN11 disease 
    ... epilepsy), vision loss, problems with balance and coordination (cerebellar ataxia), and a decline in intellectual function.Seizures ... develop another condition called GRN-related frontotemporal lobar degeneration in which cognitive decline begins between a person' ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
  10. Myoclonic epilepsy with ragged-red fibers 
    ... Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case ... Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. Eur J Hum Genet. 2012 ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
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