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Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome

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Description

Seizures, cortical blindness, and microcephaly syndrome (SCBMS) is an autosomal recessive neurodevelopmental disorder characterized by microcephaly, early-onset seizures, severely delayed psychomotor development, and cortical blindness. Affected individuals also tend to show poor overall growth with short stature (summary by Ercan-Sencicek et al., 2015).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

217

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Genes

External Links

  • OMIM

    616632

  • Orphanet

    477814

  • HPO
  • Medgen

    C4225261

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