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Microcephaly 5, primary, autosomal recessive

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Description

ASPM primary microcephaly (ASPM-MCPH) is characterized by: (1) significant microcephaly (below -3 SD for age) usually present at birth and always present before age one year and (2) the absence of other congenital anomalies. While developmental milestones are usually normal in young children, older children have variable levels of intellectual disability. Neurologic examination is usually normal except for mild spasticity. Seizures are not common.

GeneReviews

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

382

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Genes

External Links

  • OMIM

    608716

  • Orphanet
  • HPO
  • Medgen

    C1837501

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