Congenital craniostenosis with syndactyly.

Synonyms: Chotzen Syndrome, Disease, Apert-Crouzon, Saethre Chotzen Syndrome, Acrocephalosyndactyly IIIs, Syndactylic Oxycephaly, Acrocephalosyndactylies, Type 3, Acrocephalosyndactylia, Syndrome, Chotzen, Syndromes, Noack, Noack Syndrome, Type I Acrocephalosyndactylies, Acrocephalosyndactylies, Type 1, 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, Syndrome, Noack, Apert Syndrome, Type V Acrocephalosyndactyly, Pfeiffer Syndrome, Acrocephalosyndactylies, Type I, Type V Acrocephalosyndactylies, Acrocephalosyndactyly, Type III, Acrocephalosyndactyly, Type II, Noack Syndromes, Acrocephalosyndactylias, Type II Acrocephalosyndactyly, Acrocephalosyndactyly III, Type II Acrocephalosyndactylies, 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, Dysostosis Craniofacialis with Hypertelorism, Acrocephalosyndactylies, Type III, Acrocephalosyndactyly, Type 3, Syndrome, Saethre-Chotzen, Acrocephalosyndactyly, Type 1