Familial Scaphocephaly Syndrome

Familial Scaphocephaly Syndrome is related to familial scaphocephaly syndrome, mcgillivray type and scaphocephaly, maxillary retrusion, and impaired intellectual development. An important gene associated with Familial Scaphocephaly Syndrome is FGFR2 (Fibroblast Growth Factor Receptor 2). Affiliated tissues include bone.