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Myositis Ossificans (Fibrodysplasia Ossificans Progressiva)

A disease characterized by bony deposits or the ossification of muscle tissue.
Also Known As:
Fibrodysplasia Ossificans Progressiva; Myositis Ossificans Progressiva; Progressive Myositis Ossificans; Progressive Ossifying Myositis
Networked: 422 relevant articles (10 outcomes, 27 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Heterotopic Ossification (Ectopic Ossification)
2. Osteoporosis
3. Bone Resorption
4. Neoplasms (Cancer)
5. Wounds and Injuries (Trauma)

Experts

1. Kaplan, Frederick S: 46 articles (01/2022 - 01/2003)
2. Shore, Eileen M: 42 articles (01/2022 - 01/2003)
3. Pignolo, Robert J: 18 articles (01/2022 - 02/2007)
4. Bullock, Alex N: 14 articles (06/2022 - 03/2011)
5. Yu, Paul B: 13 articles (06/2022 - 03/2009)
6. Katagiri, Takenobu: 10 articles (01/2021 - 12/2008)
7. Glaser, David L: 10 articles (09/2009 - 09/2003)
8. Economides, Aris N: 9 articles (01/2022 - 12/2003)
9. Xu, Meiqi: 9 articles (01/2022 - 05/2006)
10. Hsiao, Edward C: 8 articles (12/2021 - 12/2013)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Myositis Ossificans:
1. PalovaroteneIBA
2. Etidronic Acid (HEDP)FDA LinkGeneric
3. saracatinibIBA
4. EthaneIBA
5. Serine (L-Serine)FDA Link
6. Glycine (Aminoacetic Acid)FDA LinkGeneric
03/01/2011 - "A novel ACVR1 mutation in the glycine/serine-rich domain found in the most benign case of a fibrodysplasia ossificans progressiva variant reported to date."
03/01/2011 - "Fibrodysplasia Ossificans Progressiva (FOP) is a rare, autosomal dominant condition, classically characterised by heterotopic ossification beginning in childhood and congenital great toe malformations; occurring in response to a c.617 G > A ACVR1 mutation in the functionally important glycine/serine-rich domain of exon 6. Here we describe a novel c.587 T > C mutation in the glycine/serine-rich domain of ACVR1, associated with delayed onset of heterotopic ossification and an exceptionally mild clinical course. "
06/01/2012 - "Fibrodysplasia ossificans progressiva (FOP) causes extensive heterotopic bone formation due to heterozygous mutations in the glycine-serine activation domain of ACVR1 (ALK2), a bone morphogenetic protein type I receptor. "
11/01/2009 - "Patients with classic fibrodysplasia ossificans progressiva, a disorder characterized by extensive extraskeletal endochondral bone formation, share a recurrent mutation (R206H) within the glycine/serine-rich domain of ACVR1/ALK2, a bone morphogenetic protein type I receptor. "
09/01/2007 - "Individuals with fibrodysplasia ossificans progressiva are born with malformations of the great toes and develop a heterotopic skeleton during childhood because of an identical heterozygous mutation in the glycine-serine activation domain of ACVR1, a bone morphogenetic protein type I receptor. "
7. Isotretinoin (Accutane)FDA LinkGeneric
8. SteroidsIBA
9. Anti-Bacterial Agents (Antibiotics)IBA
10. Alendronate (Alendronate Sodium)FDA LinkGeneric

Therapies and Procedures

1. Therapeutics
2. General Anesthesia
3. Intravenous Administration
4. Bone Marrow Transplantation (Transplantation, Bone Marrow)
5. Contraindications