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Article

Fibrodysplasia ossificans progressiva (FOP): watch the great toes!

European journal of pediatrics - 1 Nov 2010

Kartal-Kaess Mutlu, Shore Eileen M, Xu Meiqi, Schwering Ludwig, Uhl Markus, Korinthenberg Rudolf, Niemeyer Charlotte, Kaplan Frederick S, Lauten Melchior

Abstract excerpt

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder and the most disabling condition of heterotopic (extraskeletal) ossification in humans. Extraskeletal bone formation associated with inflammation preceding the osseous conversion usually begins in the first decade, predominantly in the head, neck, and shoulders. All patients have malformed great toes. Most patients have a spontaneous mutation...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20577760
DOI: 10.1007/s00431-010-1232-5
PMCID: PMC4964587

Genes

ACVR1

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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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