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Freeman-Sheldon syndrome

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Description

Freeman-Sheldon syndrome (FSS), or DA2A, is phenotypically similar to DA1. In addition to contractures of the hands and feet, FSS is characterized by oropharyngeal abnormalities, scoliosis, and a distinctive face that includes a very small oral orifice (often only a few millimeters in diameter at birth), puckered lips, and an H-shaped dimple of the chin; hence, FSS has been called 'whistling face syndrome.' The limb phenotypes of DA1 and FSS may be so similar that they can only be distinguished by the differences in facial morphology (summary by Bamshad et al., 2009). For a general phenotypic description and a discussion of genetic heterogeneity of distal arthrogryposis, see DA1 (108120).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

174

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Genes

External Links

  • OMIM

    193700

  • Orphanet

    2053

  • HPO
  • Medgen

    C0265224

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