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Ogden syndrome

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Description

Ogden syndrome is an X-linked neurodevelopmental disorder characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia. Many patients also have cardiac malformations or arrhythmias (summary by Popp et al., 2015).

OMIM

  • Mode of Inheritance

  • X-linked recessive inheritance
  • X-linked dominant inheritance

VARIANTS

18

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Genes

External Links

  • OMIM

    300855

  • Orphanet

    276432

  • HPO
  • Medgen

    C3275447

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