Fibrodysplasia ossificans progressiva: Clinical and genetic aspects

Robert Pignolo, Eileen M. Shore, Frederick S. Kaplan

Research output: Contribution to journalReview article

115 Citations (Scopus)

Abstract

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. Children who have FOP appear normal at birth except for congenital malformations of the great toes. During the first decade of life, sporadic episodes of painful soft tissue swellings (flare-ups) occur which are often precipitated by soft tissue injury, intramuscular injections, viral infection, muscular stretching, falls or fatigue. These flare-ups transform skeletal muscles, tendons, ligaments, fascia, and aponeuroses into heterotopic bone, rendering movement impossible. Patients with atypical forms of FOP have been described. They either present with the classic features of FOP plus one or more atypical features [FOP plus], or present with major variations in one or both of the two classic defining features of FOP [FOP variants]. Classic FOP is caused by a recurrent activating mutation (617G>A; R206H) in the gene ACVR1/ALK2 encoding Activin A receptor type I/Activin-like kinase 2, a bone morphogenetic protein (BMP) type I receptor. Atypical FOP patients also have heterozygous ACVR1 missense mutations in conserved amino acids. The diagnosis of FOP is made by clinical evaluation. Confirmatory genetic testing is available. Differential diagnosis includes progressive osseous heteroplasia, osteosarcoma, lymphedema, soft tissue sarcoma, desmoid tumors, aggressive juvenile fibromatosis, and non-hereditary (acquired) heterotopic ossification. Although most cases of FOP are sporadic (noninherited mutations), a small number of inherited FOP cases show germline transmission in an autosomal dominant pattern. At present, there is no definitive treatment, but a brief 4-day course of high-dose corticosteroids, started within the first 24 hours of a flare-up, may help reduce the intense inflammation and tissue edema seen in the early stages of the disease. Preventative management is based on prophylactic measures against falls, respiratory decline, and viral infections. The median lifespan is approximately 40 years of age. Most patients are wheelchair-bound by the end of the second decade of life and commonly die of complications of thoracic insufficiency syndrome.

Original languageEnglish (US)
Article number80
JournalOrphanet Journal of Rare Diseases
Volume6
Issue number1
DOIs
StatePublished - Dec 2 2011
Externally publishedYes

Fingerprint

Myositis Ossificans
Hallux
Aggressive Fibromatosis
Heterotopic Ossification
Virus Diseases
Type I Bone Morphogenetic Protein Receptors
Activin Receptors
Bone and Bones
Soft Tissue Injuries
Activins
Mutation
Wheelchairs
Lymphedema
Fascia
Intramuscular Injections
Genetic Testing
Osteosarcoma
Missense Mutation
Ligaments
Respiratory Tract Infections

Keywords

  • Activin A receptor type I/Activin-like kinase 2 (ACVR1/ALK2)
  • fibrodysplasia ossificans progressiva
  • heterotopic ossification
  • myositis ossificans
  • progressive osseous heteroplasia
  • toe malformation
  • trauma

ASJC Scopus subject areas

  • Genetics(clinical)
  • Pharmacology (medical)

Cite this

Fibrodysplasia ossificans progressiva : Clinical and genetic aspects. / Pignolo, Robert; Shore, Eileen M.; Kaplan, Frederick S.

In: Orphanet Journal of Rare Diseases, Vol. 6, No. 1, 80, 02.12.2011.

Research output: Contribution to journalReview article

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