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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Bibliografiske detaljer
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
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi Publishing Corporation 2013
Fag:
Case Report
Online adgang: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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