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