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Joint Hyper mobility syndrome

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https://www.readbyqxmd.com/read/27455564/-the-role-of-transforming-growth-factor-b-in-immunopathogenesis-of-diseases-of-connective-tissue
#1
REVIEW
A S Rudoi, A V Moskalev, V B Sboitchakov
The recent studies of molecular physiology of fibrillin and pathophysiology of inherent disorders of structure and function of connective tissue such as dissection and aneurysm of aorta, myxomatously altered cusps and prolapses of mitral valve, syndrome of hyper-mobility of joints, demonstrated that important role in development of these malformations play alterations of transfer of signals by growth factors and matrix cellular interaction. These conditions under manifesting Marfan's syndrome can be a consequence of anomalies of fibrillin-1 which deficiency unbrakes process of activation of transforming growth factor-β (TGFβ)...
February 2016: Klinicheskaia Laboratornaia Diagnostika
https://www.readbyqxmd.com/read/21094943/subjective-health-complaints-in-individuals-with-ehlers-danlos-syndrome-a-questionnaire-study
#2
Silje Maeland, Jörg Assmus, Britta Berglund
BACKGROUND: Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder where symptoms such as hyper mobile joints, fragile tissues, a bleeding tendency and chronic pain are frequent. Consequently, functional disability is common. OBJECTIVE: In the present study we investigated the prevalence of subjective health complaints in a Swedish EDS group. DESIGN, PARTICIPANTS AND METHOD: Members of the Swedish EDS Association were invited to respond to the questionnaire Subjective Health Complaints Inventory (SHCI)...
June 2011: International Journal of Nursing Studies
https://www.readbyqxmd.com/read/20098810/-ehlers-danlos-syndrome-with-special-emphasis-in-the-joint-hypermobility-syndrome
#3
REVIEW
Jaime F Bravo
There is an urgent need to increase the awareness on the Joint Hyper mobility Syndrome QHS). This is a congenital and prevalent emergent condition that is frequently undiagnosed and that causes significant health problems. Besides recurrent muscular-skeletal problems and signs and symptoms derived from tissue fragility, adolescents and young adults may develop osteoporosis, early osteoarthritis or dysautonomia, that are common in the disease, and deteriorate quality of life. Many JHS patients have signs and symptoms suggestive of fibromyalgia and are usually misdiagnosed...
November 2009: Revista Médica de Chile
https://www.readbyqxmd.com/read/19197843/bilateral-total-hip-arthroplasty-in-siblings-with-stickler-syndrome
#4
D Banerjee, J A Anderson, N A Taveras, A González Della Valle
Stickler Syndrome is an infrequent autosomal dominant connective tissue disorder. The most prevalent mutation affects type II collagen gene and results in abnormalities in cartilage, vitreous and nucleus pulposus. Orthopaedic manifestations include joint hyper- mobility and pain with early development of secondary osteoarthritis. The condition has a predilection for the femoral head and patients usually present in their third to fourth decade with secondary hip arthritis. We report on two siblings with Stickler Syndrome who presented with hip osteoarthritis in their third decade of life and underwent staged bilateral total hip arthroplasties (THA)...
January 2007: Hip International: the Journal of Clinical and Experimental Research on Hip Pathology and Therapy
https://www.readbyqxmd.com/read/18141960/ehlers-dalos-syndrome-syndrome-of-hyper-elastic-skin-hyper-mobile-joints-haemorrhagic-tendency-report-of-a-case
#5
B PIERARD, H PALMER
No abstract text is available yet for this article.
August 1949: New Zealand Medical Journal
https://www.readbyqxmd.com/read/15902417/musculoskeletal-manifestations-of-mild-osteogenesis-imperfecta-in-the-adult
#6
Fergus E McKiernan
The musculoskeletal manifestations of mild forms of osteogenesis imperfecta are not well defined in the adult. The aim of this study was to characterize the musculoskeletal manifestations and resulting impairments reported by adults with mild osteogenesis imperfecta. For this task a survey of musculoskeletal symptoms and impairments was hosted on the Osteogenesis Imperfecta Foundation web site for 6 weeks. Survey responses are reported herein. There were 111 unduplicated, adult respondents (78 female). Mean age was 40...
December 2005: Osteoporosis International
https://www.readbyqxmd.com/read/15375652/-neck-pain-functional-and-radiological-findings-compared-with-topical-pain-descriptions
#7
C Krasny, H Tilscher, M Hanna
Topical pain descriptions of the neck are summarized under the unspecific diagnosis "cervical syndrome" (CS). Neck pain localized in the cranial half of the cervical spine attended with occipital extension is defined as "cervicocephalic syndrome" (OCS). Pain concerning the caudal half with extention in both upper limbs or into the interscapular region is called "cervicobrachial syndrom" (UCS). The combination of both syndromes is described as "cervicocephalic and -brachial syndrom" (OUCS).The retrospective analyzed cohort of 75 patients showed a distribution of incidence of 1:20:17 of OCS : UCS : OUCS...
January 2005: Der Orthopäde
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