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Case Reports in Genetics
Volume 2013 (2013), Article ID 834605, 8 pages
http://dx.doi.org/10.1155/2013/834605
Case Report

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

1Genetics Unit, Pediatrics Department, Faculty of Medicine, Mansoura University, P.O. Box 35516, Mansoura, Egypt
2Radiology Department, Mansoura University Children's Hospital, P.O. Box 35516, Mansoura, Egypt
3Department of Anatomy and Embryology, Faculty of Medicine, Mansoura University, P.O. Box 35516, Mansoura, Egypt

Received 30 November 2012; Accepted 20 December 2012

Academic Editors: T. Hansen, S. Marquet, and X. Wang

Copyright © 2013 Mohammad Al-Haggar et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Mohammad Al-Haggar, Nermin Ahmad, Sohier Yahia, et al., “Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature,” Case Reports in Genetics, vol. 2013, Article ID 834605, 8 pages, 2013. doi:10.1155/2013/834605