Management of Knee Flexion Contracture in a Child With 3MC Syndrome Using Taylor Spatial Frame

3MC syndrome is a rare genetic disorder inherited through an autosomal recessive inheritance pattern caused by mutations in one of three genes: COLEC11, COLEC10, and MASP1. High-arched brows, ptosis, blepharophimosis, hypertelorism, cleft lip, cleft palate, developmental delay, hearing loss, abdomin...

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Detalles Bibliográficos
Autores principales: Alloqmani, Rayan A, Al-Zahrani, Mohammed S, Al-Tamimi, Gamal O, Bahmead, Emad A, Al-Rumaih, Mohammed H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Orthopedics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459810/
https://www.ncbi.nlm.nih.gov/pubmed/34589314
http://dx.doi.org/10.7759/cureus.17403

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459810/
https://www.ncbi.nlm.nih.gov/pubmed/34589314
http://dx.doi.org/10.7759/cureus.17403

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