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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Published in | Shoulder & elbow Vol. 16; no. 2; p. 169 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.04.2024
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Subjects | |
Online Access | Get more information |
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