e-ISSN 2395-3950, p-ISSN 2395-440X
e-ISSN 2395-3950, p-ISSN 2395-440X
This to certify that International Research and Publications in Medical Sciences (IRPMS) editorial team has considered to present the best paper award to the corresponding author Kristine Joy G. Boholst, Noli A. Cabildo, David Vi for publishing his outstanding research paper in IRPMS, Volume-3, Issue-4, Oct-Dec entitled as 1. FACTORS FOR TUBERCULOSIS TREATMENT RELAPSE AMONG PATIENTS PREVIOUSLY TAKING CATEGORY 1 STANDARD TUBERCULOSIS TREATMENT REGIMEN IN SELECTED MUNICIPALITIES OF ILOCOS SUR.
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Esha Sharma, Shubhangi Sharma, Rohtash K Yadav
ABSTRACT
Myositis ossificans progressiva is a rare autosomal dominant hereditary disorder, also known as Fibrodysplasia ossificans progressive (FOP) or Munchmeyer disease. Very few cases of this disorder reported worldwide. We are presenting a case of 15 year female with complaints of progressive stiffness, scoliotic deformity with restriction of movements in shoulder and elbow joint and heterotropic ossification at various sites. Early diagnosis of this disorder can be made by clinical history, examination and by imaging.
Key-words: Myositis ossificans progressiva, Hereditory disorder, Autosomal
HOW TO CITE THIS ARTICLE:
PubMed Style
Sharma E,Sharma S, Yadav RK. Myositis Ossificans Progressiva –A Case Report. IRPMS. 2017;3(3):17-20.
Vancouver/ICMJE Style
Sharma E, Sharma S, Yadav RK. Myositis Ossificans Progressiva –A Case Report. IRPMS, 2017;3(3):17-20.
Web Style
Sharma E, Sharma S, Yadav RK. Myositis Ossificans Progressiva –A Case Report. http://irpms.com/home/article_abstract/199 [Access: December 10, 2017].
AMA (American Medical Association) Style
Sharma E, Sharma S, Yadav RK. Myositis Ossificans Progressiva –A Case Report. IRPMS. 2017;3(3):17-20.
Harvard Style
Sharma E, Sharma S, Yadav RK. (2017) Myositis Ossificans Progressiva –A Case Report. IRPMS. 3(3):17-20.
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