feb 7, 1912 - Crouzon syndrome

Description:

abnormal calvarial shape: in severe case can give a "cloverleaf skull"
shallow orbits with exopthalmos
mid facial hypoplasia
bifid uvula
autosomal dominant inheritance due to a mutation in fibroblast growth factor receptor 2 (FGFR2) gene on chromosome 10q25-26.
It is named after L E Octave Crouzon, French physician

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