Results 41 to 50 of about 1,793 (201)
Fibrodysplasia ossificans progressiva: A case report
Asian Journal of Medical Sciences, 2014 Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder with unknown cause. Disease is characterized by heterotopic ossifications of connective tissue and congenital malformations of distal part of extremities.
Sreedhar Vasala
doaj +1 more source
Clinical Case Reports, Volume 7, Issue 12, Page 2526-2533, December 2019., 2019 Classical homeopathy can be included among the treatment options for congenital heterotopic ossification. Abstract Classical homeopathy can be included among the treatment options for congenital heterotopic ossification.
Dionysios Tsintzas +4 more
wiley +1 more source
When Limb Surgery Has Become the Only Life-Saving Therapy in FOP: A Case Report and Systematic Review of the Literature [PDF]
, 2020 Fibrodysplasia ossificans progressiva (FOP) is a rare disease in which heterotopic ossification (HO) is formed in muscles, tendons and ligaments. Traumatic events, including surgery, are discouraged as this is known to trigger a flare-up with risk of ...
Botman, Esmée +20 more
core +2 more sources
Myositis ossificans in a child athlete: a case study [PDF]
, 2022 Background: A 13-year-old female athlete presented with a painful lesion in her right buttock for which she had been receiving physiotherapy. It was keeping her from participating in sports.
Gounder, Perusha +10 more
core +2 more sources
Extensive Circumferential Heterotopic Ossification Discovered at the Base of a Loop Ileostomy
Case Reports in Surgery, Volume 2019, Issue 1, 2019., 2019 Heterotopic ossification is a rare phenomenon defined by the formation of bone within nonossifying soft tissues. A rare variant of heterotopic ossification is heterotopic mesenteric ossification (HMO), in which there is involvement of the mesentery and surrounding intra‐abdominal structures.
Ahmad Bosaily +6 more
wiley +1 more source
New Spontaneous Model of Fibrodysplasia Ossificans Progressiva [PDF]
, 2008 We report the first known example of spontaneous, naturally occurring fibrodysplasia ossificans progressiva (FOP) in a mammal. The Southeast Asian mouse deer of the genus _Tragulus_ (Artiodactyla: Tragulidae) have an osseous sheath covering the lower ...
Bruce Rothschild +2 more
core +1 more source
ACVR1 Gene Mutation in Sporadic Korean Patients with Fibrodysplasia Ossificans Progressiva [PDF]
, 2009 Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare but extremely disabling genetic disorder of the skeletal system, and is characterized by the progressive development of ectopic ossification of skeletal muscles and subsequent joint ...
Chin Youb Chung +20 more
core +2 more sources
American Journal of Biological Anthropology, Volume 186, Issue 3, March 2025.ABSTRACT Objectives In bioarchaeology, the concepts of resilience and frailty, and their quantification through indices, have gathered significant attention. This study is the first to apply, evaluate, and compare skeletal frailty indices and aims to trace frailty over time while identifying methodological challenges in their use on a sample ...
Petrosino +7 more
wiley +1 more source
Osteoma Cutis of the Face in CBCT Images
Case Reports in Dentistry, Volume 2017, Issue 1, 2017., 2017 Osteoma cutis (OC) is a rare benign disorder where osseous nodules form in the reticular layer of normal skin. These nodules are formed by the deposition of lamellar bone and are characterized by osteocytes in the core and osteoclasts around the periphery.
Daniah Alhazmi +5 more
wiley +1 more source
گزارش 1 مورد بيمار مبتلا به فيبروديسپلازی(ميوزيت) اسيفيکان پيشرونده [PDF]
, 2003 فيبروپلازی(ميوزيت) اسيفيکان پيشرونده بيماری نادر بافت همبند میباشد که مشخصه آن استخوانسازی نابجا در نسج نرم و بطور منتشر در تمام بدن و هالوکس والگوس دوطرفه هيپوپلاستيک(انگشت شست کوچک در پا) میباشد.
شيرانی, فاطمه
core