| Literature DB >> 27579132 |
Javaid A Muglu1, Aditya Garg2, T Pandiarajan3, Eileen M Shore4, Frederick S Kaplan5, Dhiraj Uchil6, Malcolm J Dickson3.
Abstract
Fibrodysplasia ossificans progressiva (FOP) is a rare disabling genetic disorder characterized by progressive postnatal heterotopic ossification leading to cumulative disability. Heterotopic bone formation in FOP usually begins in early childhood following a series of painful, post-traumatic, inflammatory soft-tissue swellings known as flare-ups, which later undergo ossification resulting in the progressive immobilization of the chest wall, limbs and jaw by early adulthood. Pregnancy in FOP has occurred infrequently and reproductive decisions are a dilemma for an individual or couple with FOP. We present the clinical course, medical management and potential concerns of four cases of pregnancy in FOP.Entities:
Keywords: bone morphogenetic protein; fibrodysplasia ossificans progressiva; heterotopic ossification
Year: 2011 PMID: 27579132 PMCID: PMC4989676 DOI: 10.1258/om.2011.110042
Source DB: PubMed Journal: Obstet Med ISSN: 1753-495X