Congenital craniostenosis with syndactyly.

Synonyms: Disease, Apert-Crouzon, Chotzen Syndrome, Acrocephalosyndactyly IIIs, Saethre Chotzen Syndrome, Syndactylic Oxycephaly, Acrocephalosyndactylies, Type 3, Acrocephalosyndactylia, Syndrome, Chotzen, Syndromes, Noack, Type I Acrocephalosyndactylies, Acrocephalosyndactylies, Type 1, Noack Syndrome, Type III Acrocephalosyndactyly, Acrocephalosyndactyly, Type I, Acrocephaly, Skull Asymmetry, and Mild Syndactyly, Saethre-Chotzen Syndrome, Acrocephalosyndactyly, Type V, Acrocephalosyndactylies, Type II, Syndrome, Apert, Kurczynski Casperson Syndrome, Apert Syndrome, Syndrome, Noack, Type V Acrocephalosyndactyly, Pfeiffer Syndrome, Acrocephalosyndactylies, Type I, Type V Acrocephalosyndactylies, Acrocephalosyndactyly, Type II, Acrocephalosyndactyly, Type III, Noack Syndromes, Acrocephalosyndactylias, Type II Acrocephalosyndactyly, Type II Acrocephalosyndactylies, Acrocephalosyndactyly III, Syndactylic Oxycephalies, Apert Crouzon Disease, Syndrome, Kurczynski Casperson, Syndrome, Pfeiffer, Acrocephalosyndactyly (Apert), Type I Acrocephalosyndactyly, Acrocephalosyndactylies, Type V, Apert-Crouzon Disease, Craniofacial-Skeletal-Dermatologic Dysplasia, Acrocephalosyndactylies, Type III, Dysostosis Craniofacialis with Hypertelorism, Acrocephalosyndactyly, Type 3, Syndrome, Saethre-Chotzen, Acrocephalosyndactyly, Type 1