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Aase-Smith syndrome

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Description

A very rare genetic disorder with characteristics of the following congenital malformations: hydrocephalus (due to Dandy-Walker anomaly), cleft palate and severe joint contractures. Less than 20 cases have been reported in the literature. The fingers are thin with absent knuckles and reduced creases over the joints and patients show an inability to make a full fist. Additional findings may include deformed ears, ptosis, an inability to open the mouth fully, heart defects, and clubfoot. There are currently no human genes associated with this disease.

SNOMEDCT_US

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

0

Genes

    External Links

    • OMIM

      147800

    • Orphanet

      916

    • HPO
    • Medgen

      C0220686

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