Results 71 to 80 of about 24,909 (251)

Spontaneous compartment syndrome and endovascular repair of tibioperoneal trunk pseudoaneurysm in Ehlers-Danlos syndrome

open access: yesJournal of Vascular Surgery Cases and Innovative Techniques, 2021
Vascular Ehlers-Danlos syndrome is caused by mutations in the COL3A1 (collagen type III alpha-1) gene, resulting in loss of integrity of arteries and hollow organs. Patients are predisposed to dissection, aneurysm, and organ rupture.
Krystina N. Choinski, MD   +4 more
doaj   +1 more source

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

open access: yes, 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.
Beighton   +34 more
core   +1 more source

Suspected Mitochondrial Dysfunction and Complex Pathophysiology in Fatal Hypermobile Ehlers–Danlos Syndrome: Insights from a Case Report and Post-Mortem Findings

open access: yesBiomedicines
Background/Objectives: Hypermobile Ehlers–Danlos Syndrome (hEDS) is a complex connective tissue disorder with multi-systemic manifestations that significantly impact quality of life.
Arash Shirvani   +4 more
doaj   +1 more source

The hypermobility spectrum in rugby union players, netballers and dancers: Implications for injury and performance. [PDF]

open access: yes, 2018
Armstrong Ross. The hypermobility spectrum in rugby union players, netballers and dancers: implications for injury and performance. Journal of Education, Health and Sport. 2018;8(7):269-290. eISNN 2391-8306.
Armstrong, Ross
core   +3 more sources

Ehlers-Danlos syndrome in pregnancy

open access: yesJournal of Obstetrics and Gynaecology, 2007
A 17-year-old girl with a known diagnosis of vascular type (IV) Ehlers-Danlos syndrome was seen in the antenatal clinic at 9 weeks' gestation.
S, Jaleel, K, Olah
openaire   +2 more sources

Children and adolescents with disorders of gut–brain interaction with comorbid hypermobility and orthostatic intolerance have worse outcomes

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Disorders of gut–brain interaction (DGBI) affect about 40% of children and are often comorbid with hypermobility spectrum disorders (HSDs) and orthostatic intolerance (OI). However, how these comorbidities impact outcomes in pediatric DGBI is not well understood.
Neha Santucci   +6 more
wiley   +1 more source

The prevalence of hypermobile Ehlers–Danlos syndrome at a gender-affirming primary care clinic

open access: yesSAGE Open Medicine
Objective: This study utilized a sample of trangender, nonbinary, and gender-diverse (TGD) patients to build on emerging literature that suggests that hypermobile Ehlers–Danlos syndrome may be overrepresented in TGD populations.
Theo Stein   +2 more
doaj   +1 more source

Ehlers-Danlos syndrome with infective endocarditis: A case report with literature review

open access: yesIDCases, 2019
We report a patient with Ehlers-Danlos syndrome and mitral valve infective endocarditis. The case was complicated due to multiorgan involvement and initially diagnosed as hand-foot-and-mouth disease.
Yang Jiao   +3 more
doaj   +1 more source

Which Patients With Dysfunctional Voiding Respond Well to Sacral Neuromodulation? ICI‐RS 2025

open access: yesNeurourology and Urodynamics, EarlyView.
ABSTRACT Aims Dysfunctional voiding (DV) is characterised by fluctuating or intermittent urinary flow during voiding in neurologically normal individuals. Given the different definitions used and heterogeneous pathophysiologies, outcomes following sacral neuromodulation/sacral nerve stimulation (SNM/SNS) are variably reported.
Jalesh N. Panicker   +8 more
wiley   +1 more source

Rupture of abdominal aortic aneurysm after spine surgery in the patient with Ehlers-Danlos syndrome -A case report- [PDF]

open access: yesKorean Journal of Anesthesiology, 2010
Ehlers-Danlos syndrome (EDS) is a rare inherited disorder of the connective tissue that is characterized by hyperextensible skin, hypermobile joints and abnormalities of the cardiovascular system.
Jung Sik Im   +4 more
doaj   +1 more source

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