Results 161 to 170 of about 3,792 (182)

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
openaire   +2 more sources

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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Fibrodysplasia Ossificans Progressiva

Scandinavian Journal of Rheumatology, 1977
Two cases of fibrodysplasia ossificans progressiva are reported. Both patients were females and had suffered from the disease since birth. The characteristic anomalies of great toes and thumbs associated with multiple ectopic ossifications of the connective tissue are described.
B, Hentzer, H H, Jacobsen, G, Asboe-Hansen   +2 more
openaire   +4 more sources

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
openaire   +2 more sources

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

Medizinische Genetik, 2012
Zusammenfassung Bei der Fibrodysplasia ossificans progressiva (FOP) handelt es sich um eine sehr seltene, autosomal-dominant vererbbare Erkrankung, die durch Ausbildung von heterotopen Ossifikationen charakterisiert ist, welche zu einer ausgeprägten Mobilitätseinschränkung führen.
I. Stefanova, C. Grünberg, G. Gillessen-Kaesbach   +2 more
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Fibrodysplasia (Myositis) ossificans progressiva

Seminars in Arthritis and Rheumatism, 1994
Fibrodysplasia ossificans progressiva (FOP) is a rare hereditary connective tissue disorder. Patients with FOP develop progressive ossification of muscle and connective tissue associated with pain and disability. Onset is typically in childhood, and congenital anomalies of the feet are an early sign of this condition. Pain and stiffness of the spine or
A J, Bridges, K C, Hsu, A, Singh, R, Churchill, J, Miles   +4 more
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Fibrodysplasia Ossificans Progressiva

Pathology, 2014
Fibrodysplasia ossificans progressiva (FOP) is characterized by heterotopic ossification and abnormalities of the halluces. At birth, individuals with FOP are normal except for short great toes, which can be medially deviated and monophalangic. Other more variable but common congenital abnormalities include cervical spine malformations (80 %); a short,
Stefan Mundlos, Denise Horn
openaire   +2 more sources

Fibrodysplasia Ossificans Progressiva

JCR: Journal of Clinical Rheumatology, 2021
Carlos Enrique Suárez, Acosta, Esperanza Romero, Fernández   +1 more
openaire   +2 more sources