Successful reverse total shoulder replacement in a patient with Apert syndrome

Apert syndrome, first described in the literature by a French pediatrician Eugene Apert, is a rare congenital form of acrocephalodactyly with autosomal dominant inheritance. Classically, this syndrome is characterized by craniosynostosis, midface hypoplasia, and symmetrical syndactyly of hands and f...

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Bibliographic Details
Published inShoulder & elbow Vol. 16; no. 2; p. 169
Main Authors Burton, Codey, Koong, Denis P, Seagrave, Kurt, Spasojevic, Milos, Mackenzie, Sam, Cass, Ben
Format Journal Article
LanguageEnglish
Published United States 01.04.2024
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