Arthrogryposis multiplex congenita with maxillofacial involvement: a case report

BACKGROUND: Arthrogryposis multiplex congenita is a rare condition that mainly involves the lower limbs, characterized by severe joint deformity and contracture, muscular atrophy, and functional impairment. Its clinical manifestations are heterogenous and may involve the maxillofacial district as we...

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Detalles Bibliográficos
Autores principales: Cirillo, Stefano, Regge, Daniele, Garagiola, Umberto, Tortarolo, Alessandro, Iorio, Giuseppe Carlo, Spahiu, Orges, Piancino, Maria Grazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908798/
https://www.ncbi.nlm.nih.gov/pubmed/36752944
http://dx.doi.org/10.1186/s40902-023-00378-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9908798/
https://www.ncbi.nlm.nih.gov/pubmed/36752944
http://dx.doi.org/10.1186/s40902-023-00378-6

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