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Article

Fibrodysplasia ossificans progressiva: clinical and genetic aspects.

Orphanet journal of rare diseases - 1 Dec 2011

Pignolo Robert J, Shore Eileen M, Kaplan Frederick S

Abstract excerpt

Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in characteristic extraskeletal sites. The worldwide prevalence is approximately 1/2,000,000. There is no ethnic, racial, gender, or geographic predilection to FOP....

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Source

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Identifiers

PMID: 22133093
DOI: 10.1186/1750-1172-6-80
PMCID: PMC3253727

Genes

ACVR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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