Fibrodysplasia ossificans progressiva – A rare case


Article PDF :

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Article type :

Original Article

Author :

N. S. Dhaniwala, Venkatesh Dasari, Malhar Jadhav, Vrushabh Kumbhare

Volume :

4

Issue :

2

Abstract :

Fibrodysplasia Ossificans Progressiva (FOP) also known as Myositis Ossificans Progressiva is a very rare and disabling genetic condition characterized by congenital malformation of the great toes with hallux valgus and progressive heterotopic ossification in specific anatomic pattern.1 It is a rare condition with worldwide prevalence of about 1 case in 2 million individuals2. No ethnic, racial, sex or geographical predisposition is noted. Myositis Ossificans Progressiva term is misnomer and not used now. The case report herein describes this rare condition in a child of one and half year age having the classical clinical presentation and radiological features. The child is under follow- up with measures to prevent fast progression of the condition.

Keyword :

Fibrodysplasia, Ossificans, Progressiva, Myositis.