A rare case of arthrogryposis multiplex congenita in a 2-year-old boy case report

Arthrogryposis multiplex congenita (AMC) is an uncommon condition present from birth that is marked by a combination of weakened muscles and multiple joint contractures. We present a case of a 2-year-old boy with AMC, who was born to consanguineous parents in Saudi Arabia. He presented with musculos...

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Detalles Bibliográficos
Autores principales: Waseem, Asfia, Shah, Aresha Masood, Hussain, Abbas Ali, Kumar, Sumeet, Fatima, Kiran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10524061/
https://www.ncbi.nlm.nih.gov/pubmed/37771653
http://dx.doi.org/10.1177/2050313X231200418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10524061/
https://www.ncbi.nlm.nih.gov/pubmed/37771653
http://dx.doi.org/10.1177/2050313X231200418

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