Results 51 to 60 of about 1,795 (202)
Rheumatology &Autoimmunity, Volume 5, Issue 1, Page 28-36, March 2025.Fibrodysplasia ossificans progressiva, a rare genetic disorder caused by ACVR1 mutations, leads to soft tissue ossification. Recent advancements, including food and drug administration‐approved palovarotene, show promise despite safety concerns. Therapies like tofacitinib and imatinib demonstrate potential, but larger, controlled trials are essential ...
Muhammad Ikrama +6 more
wiley +1 more source
Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
Case Reports in Orthopedics, Volume 2015, Issue 1, 2015., 2015 Juvenile Dermatomyositis (JDM) is a rare autoimmune disease in children and adolescents. In these patients calcinosis might be the most characteristic symptom. However there are only few reported cases of intramuscular calcinosis in Dermatomyositis. We report a case of calcinosis universalis (CU) of the elbow in JDM successfully treated with broaching.
Sebastian Philipp Boelch +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
Fibrodysplasia ossificans progressiva: a case report [PDF]
, 2017 Fibrodysplasia Ossificans Progressiva is a rare debilitating disorder of the musculoskeletal system affecting one in two million individuals. It is characterized by progressive extraskeletal ossification of soft tissues resulting in the original skeleton
Baidoo, Richard O., Dayie, Makafui S.
core +2 more sources
Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders
BioMed Research International, Volume 2014, Issue 1, 2014., 2014 A rare disease afflicts less than 200,000 individuals, according to the National Organization for Rare Diseases (NORD) of the United States. Over 6,000 rare disorders affect approximately 1 in 10 Americans. Rare genetic bone disorders remain the major causes of disability in US patients.
Taha Faruqi +7 more
wiley +1 more source
Miositis osificante progresiva: ultraestructura, bioquímica e histoquímica de músculo macroscópicamente sano [PDF]
, 1995 Se estudió un caso de miositis osificante progresiva en una niña de 13 años, a la cual se le tomó una muestra de músculo gastronecmio lateral, aparentemente no afectado, en el curso de una intervención quirúrgica ortopédica.
Finol, Héctor J. +4 more
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Animal models of tendon calcification: Past, present, and future
Animal Models and Experimental Medicine, Volume 7, Issue 4, Page 471-483, August 2024.Various modeling methods for experimental animal models of tendon calcification are shown in the figure: the methods of modeling tendon calcification in experimental animals as shown in the figure can be mainly classified as trauma induced, tissue factor injections, dietary or pharmacological modifications, and gene knockouts.
Ruichen Li +8 more
wiley +1 more source
Calcinosis in juvenile dermatomyositis, a therapeutic challenge [PDF]
, 2007 Calcinosis is a common and debilitating complication of dermatomyositis. It is a hallmark of the disease, occurring mainly in pediatric patients. Little is known about its pathophysiology, and there is no universally recognized treatment.
Castro, Tânia Caroline Monteiro de +4 more
core +3 more sources
Surgical excision of post-traumatic myositis ossificans of the adductor longus in a football player [PDF]
, 2020 A football player was diagnosed with myositis ossificans of his right adductor longus muscle after an acute injury. Conservative treatment failed and 1 year after the initial trauma the patient underwent surgical excision of a large ossification.
Buijk, S.E. (Steven E.) +2 more
core +3 more sources
A new spontaneous model of fibrodysplasia ossificans progressiva. [PDF]
, 2010 Fibrodisplasia ossificante progressiva (FOP) é uma doença genética caracterizada por uma acentuada, progressiva e aparentemente incontrolável ossificação dos tendões, ligamentos, faciais e músculos estriados da formação de osso heterotópico resultando na
Martin, Larry D. +2 more
core +3 more sources