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Results 1 - 6 of 6 for Stickler syndrome
  1. Stickler syndrome 
    Stickler syndrome is a group of hereditary conditions that are characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems. ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  2. Weissenbacher-Zweymüller syndrome 
    ... of two similar conditions, otospondylomegaepiphyseal dysplasia (OSMED) and Stickler syndrome type III. All of these conditions are caused ... syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome). Am J Med Genet. 1998 Nov 2;80( ...
    https://medlineplus.gov/.../weissenbacher-zweymuller-syndrome - Genetics
  3. Otospondylomegaepiphyseal dysplasia 
    ... of two similar conditions, Weissenbacher-Zweymüller syndrome and Stickler syndrome type III. All of these conditions are caused ...
    https://medlineplus.gov/.../otospondylomegaepiphyseal-dysplasia - Genetics
  4. Nonsyndromic hearing loss 
    ... others), Pendred syndrome (SLC26A4), Wolfram syndrome (WFS1), and Stickler syndrome (COL11A2). It is often unclear how mutations in ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  5. Isolated Pierre Robin sequence 
    ... organs and tissues in the body, such as Stickler syndrome or campomelic dysplasia. These instances are described as ...
    https://medlineplus.gov/.../condition/isolated-pierre-robin-sequence - Genetics
  6. Nearsightedness 
    ... night blindness, X-linked congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics