Results 21 to 30 of about 2,646,959 (190)

Generalized joint hypermobility, joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2015
This issue of the American Journal of Medical Genetics Seminar Series Part C is dedicated to generalized joint hypermobility (gJHM), joint hypermobility syndrome (JHS), and Ehlers–Danlos syndrome, hypermobility type (EDS‐HT). gJHM is the best known clinical manifestation of inherited defects of the connective tissue.
Castori, M, COLOMBI, Marina
openaire   +3 more sources

The Assessment of the Occurrence of Benign Hypermobility Joint Syndrome in Physiotherapy Students [PDF]

open access: yesCentral European Journal of Sport Sciences and Medicine, 2017
The occurrence of connective tissue disorders is an important factor for development of occupational diseases in professions requiring a non-ergonomic and often static load of the musculoskeletal system. Symptoms of the connective tissue disorders appear
Ewelina Żyżniewska-Banaszak   +5 more
doaj   +3 more sources

On the question of the syndrome of hypermobility of joints

open access: yesBolʹ, Sustavy, Pozvonočnik, 2012
This article presents the diagnostic criteria of the syndrome of joint hypermobility,  the complications of this syndrome, described therapeutic measures.
V.V. Povoroznyuk, E.I. Podlianova
doaj   +2 more sources

Chronic pain in hypermobility syndrome and Ehlers–Danlos syndrome (hypermobility type): it is a challenge

open access: yesJournal of Pain Research, 2015
Mark C Scheper,1,2 Janneke E de Vries,1–3 Jeanine Verbunt,3,4 Raoul HH Engelbert1,2 1School of Physiotherapy, Amsterdam University of Applied Sciences, Amsterdam, 2Department of Rehabilitation, Academic Medical Center, University of Amsterdam ...
Scheper MC   +3 more
doaj   +1 more source

Joint Hypermobility Syndrome in Patients With Functional Dyspepsia. [PDF]

open access: yesClin Transl Gastroenterol, 2020
INTRODUCTION: The pathophysiology underlying functional dyspepsia (FD) is multifactorial and focuses on gastric sensorimotor dysfunction. Recent studies demonstrated that joint hypermobility syndrome (JHS) is strongly associated with unexplained dyspeptic symptoms in patients attending gastrointestinal clinics ...
Carbone F, Fikree A, Aziz Q, Tack J.
europepmc   +4 more sources

[Joint hypermobility syndrome].

open access: yesActa ortopedica mexicana, 2021
Joint hypermobility syndrome is an inherited disorder with autosomal dominant pattern; is characterized by joint hyperlaxity and musculoskeletal pains. Thermal hypermobility refers to the increase in active or passive movements of joints based on their normal ranges.
N, Carbonell-Bobadilla   +5 more
openaire   +2 more sources

Joint hypermobility syndrome and dysautonomia

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Anil Kumar, Nalin Kumar Mahesh
doaj   +2 more sources

Joint hypermobility in patients with fibromyalgia syndrome [PDF]

open access: yesArthritis & Rheumatism, 1998
Abstract Objective. To test the hypothesis that joint hyperlaxity can play some role in the pathogenesis of pain in primary fibromyalgia. Methods.
M, Acasuso-Díaz, E, Collantes-Estévez
openaire   +2 more sources

The genetic basis of the joint hypermobility syndromes [PDF]

open access: yesRheumatology, 2006
Rheumatologists have long considered that joint hypermobility is inherited. The familial aggregation is striking and the pattern of inheritance strongly points to an autosomal dominant mode. The first comprehensive description of symptomatic joint hypermobility in the rheumatological literature is attributed to Kirk, Ansell and Bywaters in 1967 [1 ...
F, Malfait   +3 more
openaire   +2 more sources

Refining patterns of joint hypermobility, habitus, and orthopedic traits in joint hypermobility syndrome and Ehlers–Danlos syndrome, hypermobility type [PDF]

open access: yesAmerican Journal of Medical Genetics Part A, 2017
Joint hypermobility syndrome (JHS) and Ehlers–Danlos syndrome, hypermobility type (EDS–HT) are two overlapping heritable disorders (JHS/EDS–HT) recognized by separated sets of diagnostic criteria and still lack a confirmatory test. This descriptive research was aimed at better characterizing the clinical phenotype of JHS/EDS–HT with focus on available ...
Morlino, Silvia   +7 more
openaire   +2 more sources

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