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Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome

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Description

Smith-Kingsmore syndrome is a rare autosomal dominant syndromic intellectual disability syndrome characterized by macrocephaly, seizures, umbilical hernia, and facial dysmorphic features including frontal bossing, midface hypoplasia, small chin, hypertelorism with downslanting palpebral fissures, depressed nasal bridge, smooth philtrum, and thin upper lip (Smith et al., 2013; Baynam et al., 2015).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

23

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Genes

External Links

  • OMIM

    616638

  • Orphanet

    457485

  • HPO
  • Medgen

    C4225259

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