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Microcephaly, seizures, and developmental delay

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Description

Microcephaly, seizures, and developmental delay is an autosomal recessive neurodevelopmental disorder with onset in infancy. There is a range of phenotypic severity: some patients develop refractory seizures in infancy, consistent with a developmental and epileptic encephalopathy (DEE), whereas others have more well-controlled seizures and a more protracted course associated with cerebellar atrophy and peripheral neuropathy (Shen et al., 2010 and Poulton et al., 2013). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

87

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Genes

External Links

  • OMIM

    613402

  • Orphanet
  • HPO
  • Medgen

    C3150667

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