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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

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