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Developmental malformations-deafness-dystonia syndrome

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Description

Baraitser-Winter cerebrofrontofacial (BWCFF) syndrome is a multiple congenital anomaly syndrome characterized by typical craniofacial features and intellectual disability (ID) that ranges from mild (usually in those with normal brain structure) to profound (typically in those with a neuronal migration defect). Many (but not all) affected individuals have iris or retinal coloboma, sensorineural deafness, and muscle wasting resulting in a peculiar stance with kyphosis, anteverted shoulders, and slightly flexed elbows and knees. Seizures, congenital heart defects, and renal malformations also are common.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

6

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Genes

External Links

  • OMIM

    607371

  • Orphanet

    79107

  • HPO
  • Medgen

    C1846331

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