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Article

Fibrodysplasia ossificans progressiva: lessons learned from a rare disease.

Current opinion in pediatrics - 1 Dec 2019

Akyuz Gulseren, Gencer-Atalay Kardelen, Ata Pinar

Abstract excerpt

PURPOSE OF REVIEW: Fibrodysplasia ossificans progressiva (FOP) is an extremely rare and severely disabling autosomal dominant disease that is yet to be clearly understood. The purpose of this review is to present recent literature on pathophysiology, clinical features, diagnosis and treatment of FOP. RECENT FINDINGS: FOP is characterized by congenital great toe deformity and progressive heterotopic ossifications...

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Identifiers

PMID: 31693578
DOI: 10.1097/MOP.0000000000000802

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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