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Article

Fibrodysplasia Ossificans Progressiva.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP - 1 Feb 2016

Rashid Usman, Bari Attia, Maqsood Amna, Naz Samia, Ahmad Tahir Masood

Abstract excerpt

Fibrodysplasia Ossificans Progressiva (FOP) is a rare autosomal dominant disorder characterized by postnatal progressive heterotopic ossification of connective tissue and congenital malformation of big toes. We report a 3-year male toddler with clinical and radiological features of FOP. He was born with bilateral hallux valgus and at the age of 3 years presented with hard swellings over back, scapular region and...

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Identifiers

PMID: 26876407
DOI: 02.2016/JCPSP.154155

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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