APERT SYNDROME
Abstract:
Apert syndrome is a genetic disorder
characterized by the premature fusion of certain skull
bones (craniosynostosis). This early fusion prevents the
skull from growing normally and affects the shape of the
head and face. In addition, a varied number of fingers
and toes are fused together (syndactyly). Most cases are
sporadic, but autosomal dominant inheritance has been
reported.
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