Variants
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Autosomal recessive spinocerebellar ataxia 12

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Description

Autosomal recessive spinocerebellar ataxia-12 is a neurologic disorder characterized by onset of generalized seizures in infancy, delayed psychomotor development with mental retardation, and cerebellar ataxia. Some patients may also show spasticity (summary by Mallaret et al., 2014).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

314

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Genes

External Links

  • OMIM

    614322

  • Orphanet

    284282

  • HPO
  • Medgen

    C3280452

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