Results 61 to 70 of about 1,247,077 (145)

Hypermobile Ehlers-Danlos syndrome and rehabilitation: taking stock of evidence based medicine: a systematic review of the literature [PDF]

, 2018
[Purpose] The aim of the study was to conduct a systematic review about rehabilitation treatment of hypermobile Ehlers-Danlos syndrome, according to Evidence Based Medicine.
Gianluca Ciardi, Bruno Corrado
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, Malika Foy, Robert Carlier, Valentin Renault, Karelle Benistan   +4 more
wiley   +1 more source

Data_Sheet_1_A novel method of assessing balance and postural sway in patients with hypermobile Ehlers-Danlos syndrome.PDF

, 2023
Patients with hypermobile Ehlers-Danlos syndrome (hEDS) frequently suffer from poor balance and proprioception and are at an increased risk for falls.
Brynn Castleberry, Brittany Barker, Miguel Whitmore (16381701), Jenna Kester, Jenna Kester (16381710), Hannah Campbell (14263199), Katie Chudej, Katie Chudej (16381704), Anna Jeffcoat (16381713), Miguel Whitmore, Hannah Campbell, Thomas William Lowder, Thomas William Lowder (16381719), Ciarra Goines, Brynn Castleberry (16381716), Ciarra Goines (16381707), Anna Jeffcoat, Brittany Barker (3598370)   +17 more
core   +1 more source

Late Recognition of Suspected Ehlers‐Danlos Syndrome After Recurrent Small‐Bowel Perforations: A Case Report

Journal of General and Family Medicine, Volume 27, Issue 5, September 2026.
ABSTRACT Background Ehlers‐Danlos syndrome (EDS) may be overlooked when gastrointestinal and musculoskeletal findings are assessed separately. Case Presentation An older woman with two previous small‐bowel perforations had bilateral congenital hip dislocation, recurrent shoulder dislocations, skin hyperextensibility, and muscularis propria thinning in ...
Norio Horiguchi, Etsuko Hisanaga, Hiroko Sato, Kuniko Yoshida, Akihito Kimura, Ayumi Ito, Miki Horita, Aya Suzuki, Keiko Kawai‐Kowase   +8 more
wiley   +1 more source

Surgical management of pes planus in children with hypermobile Ehlers-Danlos: A case report and review of literature

Foot & Ankle Surgery: Techniques, Reports & Cases
Ehlers-Danlos Syndrome (EDS) is a genetic condition that affects your body's connective tissues. There are many subtypes to the disease, the most relevant to the lower extremity is hypermobile EDS.
Aaron Abraham, DPM, Robert Brarens, DPM, FACFAS   +1 more
doaj   +1 more source

Meta‐Analysis: Chronic Gastrointestinal Symptoms and Comorbidities in Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders

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, Gerald Holtmann, Thomas Fairlie, Kyle Staller, Samuel Nurko, Laurie Keefer, Douglas A. Drossman, Michael P. Jones, Qasim Aziz, Ayesha Shah   +9 more
wiley   +1 more source

Absence of the inferior labial and lingual frenula in Ehlers-Danlos syndrome

, 2001
The diagnosis of Ehlers-Danlos syndrome Is based on distinctive phenotypical characteristics such as hyperelastic skin and hypermobile joints. To date, no congenital physical markers exist for Identifying patients with Ehlers-Danlos syndrome.
DI MAGGIO, G., Franco Bagnoli, PARRINI, S., Giovanni Di Maggio, Paolo Toti, Claudio De Felice, BAGNOLI, F., Stefano Parrini, TOTI, P., DE FELICE, C.   +9 more
core   +1 more source

Parents' Experiences of Children's Healthcare for Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders [PDF]

, 2021
Hypermobile Ehlers-Danlos syndrome (hEDS) and hypermobility spectrum disorders (HSD) are underdiagnosed hereditary connective tissue disorders requiring health care across specialties.
Bell, Lauren; id_orcid, Pearce, Gemma; id_orcid, Gemma Pearce, Lauren Bell   +3 more
core   +1 more source

Surviving Their Stripes: the Diagnostic Odyssey and Impact of Life with Hypermobile Ehlers-Danlos Syndrome

Background: Hypermobile type Ehlers-Danlos Syndrome (hEDS) is subtype of Ehlers-Danlos Syndrome that is a genetic connective tissue disorder with complexities involving joint hypermobility, tissue fragility and severe pain.
Breazeale, Julianna L
core   +3 more sources

Prevalence and quality of temporomandibular disorders, chronic pain and psychological distress in patients with classical and hypermobile Ehlers-Danlos syndrome: an exploratory study

Orphanet Journal of Rare Diseases, 2023
Background The Ehlers-Danlos syndromes are a group of clinically and genetically heterogeneous hereditary diseases affecting the connective tissue. They are characterized by hypermobility of the joints, hyperextensible skin and friable tissue.
Leon Willich, Lauren Bohner, Jeanette Köppe, Jochen Jackowski, Marcel Hanisch, Ole Oelerich   +5 more
doaj   +1 more source