نتایج جستجو برای: hypermobility syndrome

تعداد نتایج: 622503  

Journal: :Journal 1989
Y Létourneau R Pérusse H Buithieu

Ehlers-Danlos syndrome is a rare hereditary disease of the connective tissue which can present oral manifestations. A brief history of the disease is presented along with the epidemiology and characteristics of the 8 main phenotypes of the syndrome. The article also describes the case of a 12-year-old patient presenting with hypermobility of the temporo-mandibular joint and capillary fragility,...

Journal: :The Journal of the American Osteopathic Association 2006
Michael R Simpson

Benign joint hypermobility syndrome (BJHS) is a connective tissue disorder with hypermobility in which musculoskeletal symptoms occur in the absence of systemic rheumatologic disease. Although BJHS has been well recognized in the rheumatology and orthopedic literature, it has not been discussed in the family medicine literature. Because most patients with musculoskeletal complaints are first se...

2015
Mark C Scheper Janneke E de Vries Jeanine Verbunt Raoul HH Engelbert

Generalized joint hypermobility (GJH) is highly prevalent among patients diagnosed with chronic pain. When GJH is accompanied by pain in ≥4 joints over a period ≥3 months in the absence of other conditions that cause chronic pain, the hypermobility syndrome (HMS) may be diagnosed. In addition, GJH is also a clinical sign that is frequently present in hereditary diseases of the connective tissue...

Journal: :American journal of medical genetics. Part C, Seminars in medical genetics 2015
Marco Castori Silvia Morlino Giulia Pascolini Carlo Blundo Paola Grammatico

Gastrointestinal involvement is a well known complication of Ehlers-Danlos syndromes (EDSs), mainly in form of abdominal emergencies due to intestinal/abdominal vessels rupture in vascular EDS. In the last decade, a growing number of works investigated the relationship between a wide spectrum of chronic gastrointestinal complaints and various EDS forms, among which the hypermobility type (a.k.a...

Journal: :American journal of medical genetics. Part C, Seminars in medical genetics 2015
Marco Castori Chiara Dordoni Silvia Morlino Isabella Sperduti Marco Ritelli Michele Valiante Nicola Chiarelli Arianna Zanca Claudia Celletti Marina Venturini Filippo Camerota Piergiacomo Calzavara-Pinton Paola Grammatico Marina Colombi

Cutaneous manifestations are a diagnostic criterion of Ehlers-Danlos syndrome, hypermobility type (EDS-HT) and joint hypermobility syndrome (JHS). These two conditions, originally considered different disorders, are now accepted as clinically indistinguishable and often segregate as a single-familial trait. EDS-HT and JHS are still exclusion diagnoses not supported by any specific laboratory te...

Journal: :Internet Journal of Rheumatology and Clinical Immunology 2015

Journal: :Al-Rafidain Journal For Sport Sciences 2012

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