Crimson Publishers Publish With Us Reprints e-Books Video articles

Abstract

Orthopedic Research Online Journal

Fibrodysplasia Ossificans Progressiva: A Case Series and Literature Review

  • Open or CloseMuhammad Naeem Shah1, Muhammad Inam2*, Imran Khan2 and Muhammad Arif3

    1Consultant Orthopedic Surgeon, Department of Orthopedic District Headquarter Hospital Temargara Lower Dir, Pakistan

    2Department of Orthopedic and Taumatology, Medical Teaching Institute Lady Reading Hopsital Peshawar, Pakistan

    3Incharge Orthopeadic unit, Hayatabad Medical Complex Peshawar, Pakistan

    *Corresponding author: Muhammad Inam, Department of Orthopedic and Taumatology, Medical Teaching Institute Lady Reading Hopsital Peshawar, Pakistan

Submission: February 25, 2022Published: March 09, 2022

DOI: 10.31031/OPROJ.2022.09.000711

ISSN : 2576-8875
Volume9 Issue3

Abstract

Fibrodysplasia Ossificans Progressiva(FOP) is a rare autosomal dominant disease, characterized by multiple bony swellings mostly in the axial musculature at shoulder. Diagnosis is based on findings of extra-skeletal ossification in the connective tissues and congenitally malformed big toe. Although the congenitally malformed big toe is present since birth, still its diagnosis is often missed. We report three cases of Fibrodysplasia Ossificans Progressiva. The patients were diagnosed one at 6 years of age, other at 10 years and other at 25 years of age. They had classical features of the disease, congenital hallux valgus deformity of foot and extra skeletal ossification. The objective of reporting these cases is to attract the researcher to do something for its prevention and treatment.

Keywords: Fibrodysplasia ossificans progressive; Hallus valgus; Ossification

Get access to the full text of this article