Results 101 to 110 of about 1,012,341 (230)
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
Multiple External Invasive Root Resorption and Calcification in Systemic Sclerosis—Case Report
International Endodontic Journal, Volume 59, Issue 9, Page 1963-1978, September 2026.ABSTRACT Aim There are few reports in the literature of multiple external invasive root resorption (EIRR) lesions in patients with systemic sclerosis (SSc), and an association between root resorption and SSc is not well established. We report the only case that comprehensively illustrates—with the combination of histopathology, cone beam computed ...
Jee‐Yun Leung +3 more
wiley +1 more source
Ehlers-Danlos syndrome type IV
, 2007 Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous ...
Germain Dominique P
core +1 more source
Ehlers–Danlos Syndrome in an Adult Woman: A Hidden Syndrome [PDF]
, 2014 Ehlers–Danlos syndrome is a rare disease and a diagnostic challenge. This case report serves to remind the clinician that it is important to identify all affected patients in order to prevent ...
Hu, Cinzia +10 more
core +1 more source
Journal of Internal Medicine, Volume 300, Issue 3, Page 299-311, September 2026.Abstract Background Postural orthostatic tachycardia syndrome (POTS) is a chronic form of orthostatic intolerance that primarily affects female patients. There are scarce data evaluating the long‐term outcomes in POTS. Objectives This study sought to evaluate the long‐term impacts of POTS over multiple decades in adult patients.
Kate M. Bourne +11 more
wiley +1 more source
Upplevelser av bemötande vid Ehlers-Danlos syndrom
, 2018 Research shows that individuals who had negative encounters in healthcare had significantly less contact with healthcare. Ehlers-Danlos syndrome is a challenge to diagnose and treat.
Jonsson, Carolina
core +1 more source
Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report
Journal of Medical Case Reports, 2013 Introduction Vascular-type Ehlers-Danlos syndrome is an autosomal dominant disease that causes arterial spurting, intestinal perforation, uterine rupture and hemopneumothorax due to decreased production of type III collagen.
Kashizaki Fumihiro +4 more
doaj +1 more source
Stroke in Ehlers-Danlos Syndrome Kyphoscoliotic Type: Dissection or Vasculitis?
, 2017 BACKGROUND: Patients with the kyphoscoliotic type of Ehlers-Danlos syndrome have an increased risk of vascular complications such as aortic dissection and perforation. Cerebral ischemia has only rarely been documented.
Martin Wiesmann +14 more
core +1 more source
EHLERS-DANLOS SYNDROME– AN OVERVIEW
International Journal of Biomedical and Advance Research, 2010 Ehlers-Danlos syndrome, hypermobility type is generally considered the least severe type of EDS, although significant complications, primarily musculoskeletal, can and do occur. The skin is often soft or velvety and may be mildly hyperextensible. Subluxations and dislocations are common; they may occur spontaneously or with minimal trauma and can be ...
openaire +3 more sources
, 2015 Ehlers-Danlos Syndrome Hypermobility Type/Joint Hypermobility Syndrome (JHS/EDS-HT) is an hereditary disorder of the connective tissue mainly manifesting with generalized joint hypermobility and skin hyperextensibility with an involvement of the ...
Claudia Celletti, Filippo Camerota
core +1 more source