Results 31 to 40 of about 2,646,959 (190)

Understanding the psychosocial impact of Joint Hypermobility Syndrome and Ehlers-Danlos Syndrome Hypermobility Type: A qualitative interview study [PDF]

open access: yes, 2019
Purpose: Little attention has been paid to psychosocial factors in Joint Hypermobility Syndrome and Ehlers–Danlos Syndrome (hypermobility type). This study sought to identify the psychosocial impact by examining participants’ lived experiences; and ...
Palmer, Shea   +4 more
core   +2 more sources

Studying the knee joint proprioception in generalized joint hypermobility as compared to healthy subjects

open access: yesمجله پژوهش در علوم توانبخشی, 2012
Introduction: The role of joint hypermobility in musculoskeletal injuries has been emphasized. In recent studies, proprioception defects have been reported in patients with hypermobility syndrome. In contrast to patients with general hypermobility, those
Abbas Yousefzadeh   +3 more
doaj   +1 more source

Síndrome da hipermobilidade articular em jovem

open access: yesGalicia Clínica, 2016
Joint hypermobility syndrome (JHS) is a hereditary connective tissue disorder characterized by symptomatic generalized joint hypermobility. Other features such as luxations and subluxations, periarticular lesions and cutaneous or other organ ...
Joana Neves   +3 more
doaj   +1 more source

Prevalence of generalized joint hypermobility in children with anxiety disorders

open access: yesBMC Musculoskeletal Disorders, 2020
Background Concerning the high prevalence of anxiety disorders and joint hypermobility in children and the lack of related studies in this age group, we aimed to assess the association of hypermobility with anxiety disorders in children.
Vadood Javadi Parvaneh   +4 more
doaj   +1 more source

Relations between the occurrence of hypermobility and gender in the group of children aged 6 - 10 years

open access: yesJournal of Education, Health and Sport, 2018
Introduction:Hypermobility of joints in healthy people may be either acquired or congenital be a symptom of a connective tissue disorder such as Marfan syndrome, osteogenesis imperfecta, or Ehler-Danlos syndrome.
Joanna Maryczkanicz   +1 more
doaj   +3 more sources

Association Between Joint Hypermobility and Pelvic Organ Prolapse: A Hospital‐Based Cross‐Sectional Study [PDF]

open access: yesHealth Sci Rep
ABSTRACT Background and Aims Pelvic organ prolapse (POP) is a prevalent disorder of the pelvic floor with multifactorial etiology. Generalized joint hypermobility (JHM) is a sign of systemic collagen laxity. This study investigated the association between generalized JHM and POP and examined other clinical correlates including parity, body mass index ...
Aziz Z.
europepmc   +2 more sources

Physical and mechanical therapies for lower limb symptoms in children with Hypermobility Spectrum Disorder and Hypermobile Ehlers-Danlos Syndrome: a systematic review

open access: yesJournal of Foot and Ankle Research, 2018
Background Hypermobility Spectrum Disorder and Hypermobile Ehlers Danlos Syndrome are two common heritable genetic disorders of connective tissue. Both conditions are characterised by excessive joint range of motion and the presence of musculoskeletal ...
Benjamin Peterson   +3 more
doaj   +1 more source

The Prevalence of Undifferentiated Connective Tissue Dysplasia in Senior Students

open access: yesReabilitacijos Mokslai: Slauga, Kineziterapija, Ergoterapija, 2023
Background. Connective tissue dysplasia is an important medical condition requiring attention and research. The aim. To analyse the prevalence of the clinical signs of undifferentiated connective tissue dysplasia among senior students of educational ...
Mykhailo Protsailo   +5 more
doaj   +1 more source

Central sensitization as the mechanism underlying pain in joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type

open access: yes, 2016
Patients with joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type (JHS/EDS-HT) commonly suffer from pain. How this hereditary connective tissue disorder causes pain remains unclear although previous studies suggested it shares similar
A. Pepe   +21 more
core   +1 more source

A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Van Maldergem syndrome (VMLDS) is an ultra‐rare autosomal recessive disorder characterized by craniofacial dysmorphism, intellectual disability, hypotonia, skeletal anomalies, and feeding difficulties. It is caused by biallelic variants in DCHS1 or FAT4 genes.
Gabriela Roldão Correia‐Costa   +4 more
wiley   +1 more source

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