Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature

Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant severe musculoskeletal disease characterized by extensive new bone formation within soft connective tissues and unique skeletal malformations of the big toes which represent a birth hallmark for the disease. Most of the isolated cl...

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Detalhes bibliográficos
Main Authors: Al-Haggar, Mohammad, Ahmad, Nermin, Yahia, Sohier, Shams, Amany, Hasaneen, Bothina, Hassan Hassan, Rasha, Wahba, Yahya, Salem, Nanees Abdel-Badie, Abdel-Hady, Dina
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2013
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3566490/
https://ncbi.nlm.nih.gov/pubmed/23424689
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/834605
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