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Late-Onset Fibrodysplasia Ossificans Progressiva (FOP) or Munchmeyer’s Disease: A Case Report and Review of Clinical and Radiological Features

Fibrodysplasia ossificans progressive (FOP) is a rare variety of myositis ossificans characterized by congenital malformations of the great toes and progressive heterotopic ossification that can induce a disabling second skeleton.
Moudatir, Mina, Younes, Dounia, Echchilali, Khadija, Lassouli, Israa, Kabli, Hassan EL   +4 more
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Fibrodysplasia ossificans progressiva [PDF]

, 2020
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Fibrodysplasia ossificans progressiva.

Indian pediatrics, 1988
K, Chopra, M M, Saha, S, Saluja
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Fibrodysplasia ossificans progressiva.

Indian pediatrics, 2006
Vedavati, Subramanyam, So, Shivbalan
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Intrathoracic Fibrodysplasia Ossificans Progressiva

The Thoracic and Cardiovascular Surgeon, 2012
Fibrodysplasia ossificans progressiva is an extremely rare disease that is usually seen in the form of sporadic cases and seems to be localized outside of the thoracic cavity. Inflammation and trauma are accused in the etiology, and too many diagnostic mistakes are done.
Alp, E, Karaoğlanoğlu, NURETTİN, Demirağ, F, Yazıcı, Ü, Özkan, S   +4 more
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Fibrodysplasia Ossificans Progressiva in China

Bone, 2018
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare and devastating disorder characterized by cumulative episodes of progressive heterotopic ossification. It is estimated that there exist 600-700 patients in Mainland China. Nevertheless, due to the rarity, many FOP patients were initially misdiagnosed.
Dunmin She
exaly   +3 more sources

Fibrodysplasia ossificans progressiva

Pediatric Radiology, 2001
Fibrodysplasia ossificans progressiva (FOP) is an extremely rare and disabling genetic disorder of connective tissue. The condition is characterized by congenital malformation of the great toes and by progressive heterotopic ossification of the tendons, ligaments, fasciae, and striated muscles.
S, Mahboubi, D L, Glaser, E M, Shore, F S, Kaplan   +3 more
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Fibrodysplasia ossificans progressiva

The Indian Journal of Pediatrics, 2004
A 2-year-old boy presented with low-grade fever and multiple progressive painful swellings over upper dorsal trunk and supraclavicular region with progressive stiffening of skin for the last 2 months. Examination revealed dysmorphic face, proximally placed thumb and bilateral hallux valgus.
L, Subramanyam, Kalpana, Gowrishankar, So, Shivbalan, A, Balachandran   +3 more
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Fibrodysplasia ossificans progressiva

American Journal of Roentgenology, 1982
Three hundred fifty-three previously reported cases of fibrodysplasia ossificans progressiva were reviewed and six new cases were analyzed radiologically. Characteristic findings of fibrodysplasia ossificans progressiva were confirmed and radiographic signs of the disease were demonstrated, including medial cortical thickening of the proximal tibia ...
D, Thickman, A, Bonakdar-pour, M, Clancy, J, Van Orden, H, Steel   +4 more
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Advanced Fibrodysplasia Ossificans Progressiva

Clinical Nuclear Medicine, 1995
Fibrodysplasia ossificans progressiva is a rare hereditary variant of heterotropic bone formation that is often difficult to diagnose. A bone scan of an advanced case of this condition is presented. Nuclear medicine physicians should be familiar with various aspects of this disease.
A H, Elgazzar, V M, Kriss, M J, Gelfand
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