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Results 1 - 10 of 54 for Cerebellar atrophy
  1. Multiple system atrophy - cerebellar subtype 
    Multiple system atrophy - cerebellar subtype (MSA-C) is a rare disease that causes areas deep in the brain, just above the spinal ... MSA-C used to be known as olivopontocerebellar atrophy (OPCA).
    https://medlineplus.gov/ency/article/000758.htm - Medical Encyclopedia
  2. Pontocerebellar hypoplasia 
    Pontocerebellar hypoplasia is a group of related conditions that affect the development of the brain. The term "pontocerebellar" refers to the pons and the cerebellum, ...
    https://medlineplus.gov/.../condition/pontocerebellar-hypoplasia - Genetics
  3. Pol III-related leukodystrophy 
    ... part of the brain involved in coordinating movements (cerebellar atrophy) and underdevelopment (hypoplasia) of tissue that connects the ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  4. Spinocerebellar ataxia type 36 
    ... affected by expansion of the gene, leading to cerebellar atrophy. Deterioration in this part of the brain leads ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  5. Microcephaly, seizures, and developmental delay 
    ... de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  6. Schimke immuno-osseous dysplasia 
    ... Das AM, Knauth M, Becker H, Donnerstag F. Cerebellar atrophy in Schimke-immuno-osseous dysplasia. Am J Med ...
    https://medlineplus.gov/.../schimke-immuno-osseous-dysplasia - Genetics
  7. POLR3B gene 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because ...
    https://medlineplus.gov/genetics/gene/polr3b - Genetics
  8. PNKP gene 
    ... de Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  9. EXOSC3 gene 
    ... family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3. Neurogenetics. 2013 ...
    https://medlineplus.gov/genetics/gene/exosc3 - Genetics
  10. POLR3A gene 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
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