Results 51 to 60 of about 1,081,004 (187)
SSM: Qualitative Research in Health, 2023 Patients with hypermobile Ehlers Danlos Syndrome often experience psychological distress resulting from the perceived hostility and disinterest of their clinicians.
Colin M.E. Halverson +2 more
doaj +1 more source
Cardiovascular autonomic dysfunction in Ehlers–Danlos syndrome—Hypermobile type [PDF]
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017 Autonomic dysfunction contributes to health‐related impairment of quality of life in the hypermobile type of Ehlers–Danlos syndrome (hEDS). Typical signs and symptoms include tachycardia, hypotension, gastrointestinal dysmotility, and disturbed bladder function and sweating regulation.
Alan, Hakim +5 more
openaire +2 more sources
, 2022 BackgroundPeople with Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders are hampered in their social participation, especially in the social relationships they have.ObjectiveThe aim of this study is to research the impact of hypermobile Ehlers-
Fransiska Malfait (221447) +7 more
core +1 more source
Oral Manifestations of Non Vascular Ehlers‐Danlos Syndrome Cross‐Sectional Study
Oral Diseases, EarlyView.ABSTRACT Background Ehlers–Danlos syndromes are rare hereditary connective tissue disorders; however, their oral manifestations remain poorly characterized in molecularly confirmed individuals. The aim of this study was to describe the oral phenotype of patients with non‐vascular Ehlers‐Danlos syndromes compared to healthy controls.
Aude Grand +4 more
wiley +1 more source
Solitary Lesion With Features of Atrophic Papulosis in Early Childhood
Pediatric Dermatology, EarlyView.ABSTRACT Atrophic papulosis (Köhlmeier‐Degos disease) is a rare thrombo‐occlusive vasculopathy classically presenting with multiple porcelain‐white atrophic papules and a high risk of progression to systemic involvement. We report a 2‐year‐old girl presenting with clinical, dermoscopic, and histologic findings of atrophic papulosis with only a solitary
Ou Jia Emilie Wang +4 more
wiley +1 more source
, 2020 Objectives: To investigate the prevalence of joint hypermobility classes, hypermobility spectrum disorders,hypermobile Ehlers-Danlos syndrome and their relations with sex ina university population.
Filiz TUNA, Tuna, Filiz
core +1 more source
Vascular Abnormalities in Hypermobile Ehlers–Danlos Syndrome: A Retrospective Cohort Study
American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2080-2087, September 2026.ABSTRACT Hypermobile Ehlers–Danlos syndrome (hEDS), while generally free from severe vascular complications, may occasionally present with cardiac and vascular abnormalities that warrant specific investigation. While studies have been conducted on the prevalence of cardiac involvement, none have focused on vascular aspects. This retrospective study was
Thomas Gehin +4 more
wiley +1 more source
Classification, nosology and diagnostics of Ehlers-Danlos syndrome
Journal of Biomedicine and Translational Research, 2019 Ehlers-Danlos syndrome (EDS) comprises a group of heritable connective tissue disorders which has as cardinal features varying degrees of skin hyperextensibility, joint hypermobility, easy bruising and skin fragility.
Ben C J Hamel
doaj +1 more source
Clinical Case Reports, 2019 Key Clinical Message Hypermobile type Ehlers‐Danlos syndrome (hEDS) is an underdiagnosed connective tissue disorder characterized by generalized joint hypermobility, chronic fatigue, widespread joints pain, and impaired quality of life. Here, we reported
Wei Zhang +3 more
doaj +1 more source
Alimentary Pharmacology &Therapeutics, Volume 64, Issue 5, Page 574-589, September 2026.This meta‐analysis reveals that a significant proportion of patients with hEDS/HSD experience gastrointestinal symptoms. The most prevalent symptoms include heartburn, abdominal pain, constipation, and nausea. There is a notable overlap of hEDS/HSD with chronic fatigue, DGBI, GERD, migraine, and orthostatic intolerance.
Dmitrii Kulin +9 more
wiley +1 more source