TY - JOUR T1 - Yetişkin Bir Hintli Erkekte Progresif Ossifikan Fibrodisplazi TT - Fibrodysplasia Ossificans Progressiva in an Adult Indian Male AU - Harjai, Rachit AU - Kachewar, Sushil Ghanshyam PY - 2014 DA - December DO - 10.17826/cutf.55160 JF - Cukurova Medical Journal JO - Cukurova Med J PB - Çukurova Üniversitesi WT - DergiPark SN - 2602-3032 SP - 0 VL - 39 IS - 4 LA - tr AB - İlk olarak 1692 yılında Guy Patin tarafından kadınları ahşaba dönüştüren hastalık olarak tanımlanmasını takiben Progresif Ossifikan Fibrodisplazi, bir çok kitapta genelde olarak düşük bir profil muhafaza etmiş ve nadiren bu durum tarafından etkilenen yaşayan bireylere rastlanmıştır. Bu ölümcül hastalığın işaretleri sadece büyük ayak baş parmağının kısalığı ve yumuşak dokuların engellenemeyen progresif kemikleşmesidir. Sporadik oluşuma sahip olabilir, hatta otozomal dominant pattern yoluyla kalıtılabilir ve geniş bir ifade yelpazesine sahip olabilir. Yanlış bir klinik tanı hastayı gereksiz cerrahi eksizyona ve hatta zararlı radyoterapiye maruz bırakır. Yetişkin Hintli erkeklerdeki Progresif Ossifikan Fibrodisplazi vakasına bağlı durum, herkesin yararı için burada rapor edilmiştir. KW - Münchmeyer hastalığı KW - Progresif Ossifikan Fibrodisplazi KW - Kalsifikasyonlar KW - Kısa KW - büyük ayak baş parmağı KW - Paraspinal kemikleşme KW - Mikrodaktili; Simfalangizm N2 - Following its first description by Guy Patin in 1692 as a disease that turned a woman into wood, Fibrodysplasia Ossificans Progressiva has maintained its low profile that too mainly in textbooks and rarely does one encounter a live walking individual affected by this entity. The hallmarks of this deadly disease are the short size of only the big toes and uninhibited progressive ossification of soft tissues. It can have a sporadic occurrence or may even be inherited through autosomal dominant pattern and has a wide range of expression. A wrong clinical diagnosis exposes the patient to unnecessary surgical excision and even harmful radiotherapy.Hence a case of Fibrodysplasia Ossificans Progressiva in an adult Indian male is being reported here for the benefit of one and all. CR - Illingworth, RS. Myositis OssificansProgressiva (Munchmeyer's Disease), Archives of Disease in Childhood 1971;46:264. CR - Kaplan, FS; Glaser, DL; Hebela, N; Shore, EM. Heterotropic Ossification. Journal of the American Academy of Orthopedic Surgeons. 2004;12:116-125. CR - Rogers, JG; Geho, WB. FibrodysplasiaOssificansProgressiva. J Bone joint Surg (Am). 1979;61:909. CR - Connor, JM; Evans, DAP. FibrodysplasiaOssificansProgressiva. The Clinical Features and Natural History of 34 Patients. The Journal of Bone and Joint Surgery. 1982;64:76-83. CR - Meij, EH; van der Becking, AG; Waal, I van der. FibrodysplasiaOssificans progressive. An unusual cause of restricted mandibular movement. Oral Diseases. 2005;12:204-7 CR - Kingsley, DM. the TGF-b super family: new members, new receptors and new genetic tests of function in different organisms. Genes Development. 1994;8:133-46. CR - Kachewar SG, Sankaye SB and Kulkarni DS. The role of Radio-diagnosis in Inborn Errors of Metabolism. Journal of Clinical and Diagnostic Research. 2011;5:1467-72. CR - Kingsley, DM. What do BMPs do in mammals? Clues from the mouse short ear mutation. TIG. 1994;10:16 CR - Smith, R; Athanasou, NA; Vipond, SE; Fibrodysplasia (myositis) Ossificansprogressiva: clinic-pathological features and natural history, the Nuffield Orthopaedic Centre, Headington, Oxford, UK, Q J Med. 1996;89:445-56. CR - Kachewar SG, Sankaye SB. Reviewer index: a new proposal of rewarding the reviewer.Mens Sana Monogr. 2013;11:274-84. CR - Lanchoney, TF; Olmstead, EA; Shore, EM; et al. Characterization of bone morphogenetic protein 4 receptor in Fibrodysplasiaossificansprogressiva. Clinorthop. 1998;346:38- 45. CR - Kaplan, FS; Glaser, DL; Hebela, N; Shore, EM. Heterotropic Ossification. Journal of the American Academy of Orthopedic Surgeons 2004;12:116-25. CR - YazışmaAdresi / Address for Correspondence: Dr. Rachit Harjai Mahatma Gandhi Medical College and Hospital, i Jaipur, INDIA Email: radsgk@gmail.com. G eliştarihi/Received on : 06.01.2014 CR - Kabul tarihi/Accepted on: 14.02.2014 UR - https://doi.org/10.17826/cutf.55160 L1 - https://dergipark.org.tr/tr/download/article-file/47102 ER -