Congenital craniostenosis with syndactyly.

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