Apert syndrome |
Acrocephalosyndactyly (Apert); Acrocephaly |
Apert Syndrome, virtually synonymous with Acrocephalosyndactyly, is a branchial arch syndrome, characterized by a number of clinical features, resulting from a developmental anomaly. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Since the branchial arches are important developmental features in a growing embryo, disturbances in its development create lasting and widespread effects. Overview In 1906, Eugè ...
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- Genetics Home Reference: Apert syndrome (Genetics Home Reference)

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