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Results 1 - 3 of 3 for Apert syndrome
  1. Apert syndrome 
    Apert syndrome is a genetic disorder characterized by skeletal abnormalities. A key feature of Apert syndrome is the premature closure of the bones of the ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  2. FGFR2 gene 
    ... the FGFR2 gene have been found to cause Apert syndrome. This condition causes premature closure of the bones ... symptoms.More than 98 percent of cases of Apert syndrome are caused by one of two mutations in ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  3. Crouzon syndrome 
    ... Becchetti A, Carinci P, Baroni T, Bodo M. Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix. J Craniofac ...
    https://medlineplus.gov/genetics/condition/crouzon-syndrome - Genetics