Results 81 to 90 of about 1,232,690 (211)

Pregnancy outcome in joint hypermobility syndrome and Ehlers–Danlos syndrome

open access: yes, 2017
IntroductionAn increased risk of preterm birth in women with joint hypermobility syndrome or Ehlers-Danlos syndrome is suspected. Material and methodsIn this nationwide cohort study from 1997 through 2011, women with either joint hypermobility syndrome ...
Jonas F. Ludvigsson   +12 more
core   +1 more source

Venous insufficiency after prolonged standing: Is joint hypermobility an important risk factor?

open access: yesAdvanced Biomedical Research, 2015
Background: Varicose veins are extremely common disease which is due to elevated superficial venous pressures. We aimed to know that if joint hypermobility causes the venous insufficiency following the prolonged standing.
Kamran Azma   +4 more
doaj   +1 more source

Beyond Joint Hypermobility: Investigating Bladder Dysfunction in Hypermobile Ehlers‐Danlos Syndrome

open access: yesNeurourology and Urodynamics, Volume 45, Issue 8, Page 1687-1691, November 2026.
ABSTRACT Introduction and Objectives Hypermobile Ehlers‐Danlos Syndrome (hEDS) is the most common subtype of Ehlers‐Danlos Syndrome, a group of connective tissue disorders caused by collagen abnormalities. While musculoskeletal features of hEDS are well characterized, its impact on visceral organs, including the bladder, remains underexplored.
Marium Ansari   +5 more
wiley   +1 more source

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas–Mexico Border

open access: yesClinical Genetics, Volume 110, Issue 5, Page 627-636, November 2026.
Project GIVE provided evaluations and genome sequencing to 23 children with hearing loss along the Texas–Mexico border. Seventy percent received a molecular diagnosis and 56% of those diagnosed had changes to medical management. In this region, underdiagnosis of genetic hearing loss is due to care barriers rather than lower genetic burden.
Desiree Lanehart   +17 more
wiley   +1 more source

Gastrointestinal disorders in joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type: A review for the gastroenterologist [PDF]

open access: yes, 2017
BackgroundJoint hypermobility syndrome (JHS)/Ehlers-Danlos syndrome hypermobility type (EDS-HT) is the most common hereditary non-inflammatory disorder of connective tissue, characterized by a wide range of symptoms, mainly joint hyperextensibility and ...
Vork, L.   +6 more
core   +2 more sources

Carotid artery dissection linked to intermittent apnoeic swimming: A case–control study

open access: yesExperimental Physiology, Volume 111, Issue 11, Page 4966-4978, 1 November 2026.
Abstract Internal carotid artery (ICA) dissection is a rare and potentially devastating cause of cerebral ischaemia, initiated by an intimal tear or rupture of the vasa vasorum, that can lead to an intraluminal thrombus, vascular stenosis, occlusion, or dissecting aneurysm formation.
Damian M. Bailey   +14 more
wiley   +1 more source

Benign hypermobility syndrome in Greek schoolchildren

open access: yes, 2000
Since the incidence of benign hypermobility syndrome is significantly high in otherwise healthy children, paediatricians should consider this benign entity when they evaluate musculoskeletal complaints in ...
Tsanaktsi, M, Moustaki, M, Vougiouka, O
core  

Relationship between fatigue and gait abnormality in Joint Hypermobility Syndrome/Ehlers-Danlos Syndrome Hypermobility type

open access: yes, 2012
Ehlers-Danlos syndrome (EDS) is a clinically and genetically heterogeneous group of inherited connective tissue disorders characterised by joint hypermobility, skin hyperextensibility and tissue fragility.
F. Camerota   +11 more
core   +1 more source

Corrigendum to "Folate-dependent hypermobility syndrome: A proposed mechanism and diagnosis" [Heliyon 9 (4), (April 2023) Article e15387]. [PDF]

open access: yesHeliyon, 2023
Courseault J   +7 more
europepmc   +1 more source

Prolonged standing behaviour in people with joint hypermobility syndrome. [PDF]

open access: yesBMC Musculoskelet Disord, 2021
Bates AV, McGregor AH, Alexander CM.
europepmc   +1 more source

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