Results 1 to 10 of about 50 (39)

Fibrodysplasia ossificans progressiva [PDF]

Best Practice & Research Clinical Rheumatology, 2008
Fibrodysplasia ossificans progressiva (FOP), a rare and disabling genetic condition of congenital skeletal malformations and progressive heterotopic ossification (HO), is the most catastrophic disorder of HO in humans. Episodic disease flare-ups are precipitated by soft tissue injury, and immobility is cumulative.
Frederick S, Kaplan, Martine, Le Merrer, David L, Glaser, Robert J, Pignolo, Robert E, Goldsby, Joseph A, Kitterman, Jay, Groppe, Eileen M, Shore   +7 more
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Fibrodysplasia ossificans progressiva

Clinical Case Reports, 2023
Fibrodysplasia ossificans progressiva is a rare condition with an estimated prevalence of one in two million individuals. The condition is characterised by widespread heterotrophic ossification of skeletal muscles and ligaments. We report the case of an eight-year-old female patient and show the radiological progression of the condition.
Chané Smit, André Uys
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Pregnancy in fibrodysplasia ossificans progressiva [PDF]

Obstetric Medicine, 2011
Fibrodysplasia ossificans progressiva (FOP) is a rare disabling genetic disorder characterized by progressive postnatal heterotopic ossification leading to cumulative disability. Heterotopic bone formation in FOP usually begins in early childhood following a series of painful, post-traumatic, inflammatory soft-tissue swellings known as flare-ups ...
Javaid A, Muglu, Aditya, Garg, T, Pandiarajan, Eileen M, Shore, Frederick S, Kaplan, Dhiraj, Uchil, Malcolm J, Dickson   +6 more
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FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

British Journal of Anaesthesia, 1990
A 14-yr-old boy with fibrodysplasia ossificans progressiva (FOP) presented for surgery for bilateral division of his ossified masseter muscles. Patients with FOP may present problems to the anaesthetist, including difficulties with tracheal intubation, restrictive pulmonary disease and abnormalities of cardiac conduction.
M C, Newton, P W, Allen, D C, Ryan
openaire   +2 more sources

Fibrodysplasia Ossificans Progressiva

Annals of Saudi Medicine, 1999
Fibrodysplasia ossificans progressiva (FOP) is a rare disorder. The striking features of the disorder are the replacement of muscles, tendons, and aponeuroses by masses of bone, and the presence of certain skeletal abnormalities. In this report, we describe a woman who has literally grown up in bed since the age of three years.
A H, Zargar, B A, Laway, S R, Masoodi, A I, Wani, M I, Bashir, M M, Wani   +5 more
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Fibrodysplasia ossificans progressiva.

Neurology India
Abstract: Fibrodysplasia Ossificans Progressiva (FOP), commonly known as Stoneman Syndrome, is an ultra-rare genetic disorder characterized by the progressive ossification of soft tissues, leading to the formation of a secondary skeleton. This paper provides a comprehensive analysis of FOP, examining its epidemiology, pathophysiology, clinical ...
P, Garg, S, Jain, R, Khadgawat, B, Choudhary, S, Gupta, S, Burad   +5 more
openaire   +3 more sources

Fibrodysplasia ossificans progressiva.

JPMA. The Journal of the Pakistan Medical Association, 2011
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder of the connective tissue characterized by progressive disability as a result of extensive extra skeletal enchondral bone formation and malformed big toes which are often monophalangic.
Nadia, Shaikh, Fehmina, Arif
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Fibrodysplasia ossificans progressiva [PDF]

The Indian Journal of Pediatrics, 1994
S, Ganguly, D K, Paul, B, Ghosal, A, Choube   +3 more
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Fibrodysplasia Ossificans Progressiva (FOP) [PDF]

Journal of Bone and Mineral Research, 1997
F S, Kaplan, R M, Smith
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Fibrodysplasia ossificans progressiva

Rheumatology, 2019
Uma Kumar, Shiv Kumar Suman, Sauvik Dasgupta, Rajiv Ranjan Kumar   +3 more
openaire   +2 more sources