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  • Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial
  • this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
  • Mutations in the COL11A1 gene account for 10 to 20 percent of all cases of Stickler syndrome. When
  • described below) and to a form of Stickler syndrome classified as type III. In some cases, it can be
  • significantly overlap those of two similar conditions, otospondylomegaepiphyseal dysplasia (OSMED) and Stickler
  • overlap those of two similar conditions, Weissenbacher-Zweymüller syndrome and Stickler syndrome type III
  • Stickler syndrome or campomelic dysplasia. These instances are described as syndromic. When Pierre Robin
  • Almost 200 mutations in the COL2A1 gene have been found to cause the most common form of Stickler
  • Stickler Involved People
  • syndrome (SLC26A4), Wolfram syndrome (WFS1), and Stickler syndrome (COL11A2). It is often unclear how