FIBRODYSPLASIA OSSIFICANS PROGRESSIVE: A CASE REPORT

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OLADNABI M.; HADDADI T.; KIANMEHR A.; MANSOUR SAMAEI N.; AGHAIE M.

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Journal: JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES Year:2017 | Volume:19 | Issue:3 (63) Page(s): 111-115

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Title

FIBRODYSPLASIA OSSIFICANS PROGRESSIVE: A CASE REPORT

Author(s)

Keywords

FIBRODYSPLASIA OSSIFICANS PROGRESSIVAQ1

ACVR1Q1

AUTOSOMAL DOMINANTQ3

Abstract

FIBRODYSPLASIA OSSIFICANS PROGRESSIVA (FOP) is an extremely rare AUTOSOMAL DOMINANT disorder having variable expressivity with complete penetrance. FOP incidence has been estimated to be 1 per 2 million. FOP caused by mutations in ACVR1 gene encoding bone morphogenetic protein type-1 receptor. To date, 15 types of mutations have been reported. The majority of cases were determined to be the rsult of a new mutation occuring sporadically. Here we report a 20 years old girl who's suffering FOP for 11 years.

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APA: Copy

OLADNABI, M., HADDADI, T., KIANMEHR, A., MANSOUR SAMAEI, N., & AGHAIE, M.. (2017). FIBRODYSPLASIA OSSIFICANS PROGRESSIVE: A CASE REPORT. JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES, 19(3 (63) ), 111-115. SID. https://sid.ir/paper/79007/en

Vancouver: Copy

OLADNABI M., HADDADI T., KIANMEHR A., MANSOUR SAMAEI N., AGHAIE M.. FIBRODYSPLASIA OSSIFICANS PROGRESSIVE: A CASE REPORT. JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2017;19(3 (63) ):111-115. Available from: https://sid.ir/paper/79007/en

IEEE: Copy

M. OLADNABI, T. HADDADI, A. KIANMEHR, N. MANSOUR SAMAEI, and M. AGHAIE, “FIBRODYSPLASIA OSSIFICANS PROGRESSIVE: A CASE REPORT,” JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES, vol. 19, no. 3 (63) , pp. 111–115, 2017, [Online]. Available: https://sid.ir/paper/79007/en

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