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Results 11 - 20 of 33 for Progressive cerebellar ataxia
  1. Primary coenzyme Q10 deficiency 
    ... a person's sixties and often cause cerebellar ataxia, which refers to ... muscle stiffness (spasticity), abnormal eye movements (nystagmus), vision ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  2. Mainzer-Saldino syndrome 
    ... of scar tissue in the liver (hepatic fibrosis); cerebellar ataxia, which is difficulty with coordination and balance arising ... Saldino disease MZSDS Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia Saldino-Mainzer dysplasia Saldino-Mainzer ...
    https://medlineplus.gov/genetics/condition/mainzer-saldino-syndrome - Genetics
  3. Microcephaly, seizures, and developmental delay 
    ... van de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  4. PNKP gene 
    ... van de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  5. Myoclonic epilepsy with ragged-red fibers 
    ... Kay CK, Raskin S, Werneck LC, Bruhn H. Cerebellar ataxia, myoclonus, cervical lipomas, and MERRF syndrome. Case report. ...
    https://medlineplus.gov/...myoclonic-epilepsy-with-ragged-red-fibers - Genetics
  6. Charcot-Marie-Tooth disease 
    ... DISEASE, X-LINKED RECESSIVE, 4, WITH OR WITHOUT CEREBELLAR ATAXIA; CMTX4 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  7. Multiple system atrophy 
    ... atrophy, known as MSA-C, is characterized by cerebellar ataxia, which causes problems with coordination and balance. This ...
    https://medlineplus.gov/genetics/condition/multiple-system-atrophy - Genetics
  8. CLN11 disease 
    ... epilepsy), vision loss, problems with balance and coordination (cerebellar ataxia), and a decline in intellectual function.Seizures in ...
    https://medlineplus.gov/genetics/condition/cln11-disease - Genetics
  9. Spinocerebellar ataxia type 1 
    ... Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1. Cerebellum. 2008;7(2):106-14. doi: 10.1007/s12311-008-0009-0. Citation on PubMed Zoghbi HY, Orr HT. Pathogenic mechanisms ... disease, spinocerebellar ataxia type 1. J Biol Chem. 2009 Mar 20; ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-1 - Genetics
  10. Spinocerebellar ataxia type 2 
    ... Lastres-Becker I, Rub U, Auburger G. Spinocerebellar ataxia 2 (SCA2). Cerebellum. 2008;7(2):115-24. doi: 10.1007/s12311-008-0019-y. Citation on PubMed Mederos LE, Proenza CL, Almira ... counseling for spinocerebellar ataxia type 2. Clin Genet. 2008 Dec;74(6): ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-2 - Genetics
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