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Microcephalic primordial dwarfism due to ZNF335 deficiency

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Description

Primary microcephaly-10 (MCPH10) is an autosomal recessive disorder characterized by extremely small head size (-9 SD) at birth and death usually by 1 year of age. Neuropathologic examination shows severe loss of neurons as well as neuronal loss of polarity and abnormal dendritic maturation (summary by Yang et al., 2012). For a general phenotypic description and a discussion of genetic heterogeneity of primary microcephaly, see MCPH1 (251200).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

13

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Genes

External Links

  • OMIM

    615095

  • Orphanet

    329228

  • HPO
  • Medgen

    C3554499

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