Results 161 to 170 of about 1,081,004 (187)

Echocardiographic findings in classical and hypermobile Ehlers–Danlos syndromes

American Journal of Medical Genetics Part A, 2005
AbstractStructural cardiovascular alterations in the classical and hypermobile forms of Ehlers–Danlos syndrome(EDS) warrant investigation. We have examined a cohort of 38 patients with hypermobile and classical EDSs using two‐dimensional echocardiography. The cohort includes 7 males and 31 females, with an age range from 12–60 years.
Nazli B, McDonnell, Beverly L, Gorman, Katherine W, Mandel, Shepherd H, Schurman, Alison, Assanah-Carroll, Susan A, Mayer, Samer S, Najjar, Clair A, Francomano   +7 more
openaire   +2 more sources

Orthopaedic Manifestations in Hypermobile Ehlers-Danlos Syndrome

Journal of Bone and Joint Surgery
Background: Hypermobile Ehlers-Danlos syndrome (hEDS) is a collagen disorder affecting multiple organ systems, including the musculoskeletal system. We sought to determine the type and severity of orthopaedic manifestations experienced by these patients.
Josef K. Eichinger, Rebecca L. Byrd, Evan P. Bailey, Robert J. Reis, Victoria Daylor, Maggie Schiessl, Cortney Gensemer, Richard J. Friedman, Sunil J. Patel, Russell A. Norris   +9 more
openaire   +2 more sources

Hippotherapy in the management of hypermobile Ehlers-Danlos syndrome

BMJ Case Reports
Hypermobile Ehlers-Danlos syndrome (EDS) is an inherited condition marked by joint hypermobility, instability, chronic pain and fatigue, significantly impacting quality of life and autonomy. Management focuses solely on symptom alleviation. After experiencing a rapid decline in functional abilities, a patient in late adolescence with hypermobile EDS ...
Hélène Viruega, Célia Loriette, Melissa Quignon, Manuel Gaviria   +3 more
openaire   +2 more sources

Abdominal Compression Syndromes in the Hypermobile Ehlers‐Danlos Syndrome

American Journal of Medical Genetics Part A
ABSTRACT The median arcuate ligament syndrome (MALS) is the main cause of abdominal compression syndromes (ACS). Diagnosis is frequently missed for many years despite the unremitting epigastric and left upper abdominal quadrant pain, postprandial pain, postural relief, sitophobia, and weight loss.
Aubrey Milunsky, Jeff M. Milunsky, Richard Hsu   +2 more
openaire   +2 more sources

Predictors of pain and mobility disability in the hypermobile Ehlers-Danlos syndrome

Disability and Rehabilitation, 2019
Aim: Among the Ehlers-Danlos syndromes, the hypermobile subtype (hEDS) is the most common. The variety, accumulation and duration of the painful symptoms make hEDS a chronic and highly disabling condition. Identifying drivers of pain and mobility disability in hEDS is necessary to provide adapted prevention and intervention programs.Methods: A cross ...
Kalisch, Larissa, Hamonet, Claude, Bourdon, Caroline, Montalescot, Lucile, de Cazotte, Cécile, Baeza-Velasco, Carolina   +5 more
openaire   +2 more sources

Patient perspectives on employment participation in the “hypermobile Ehlers–Danlos syndrome”

Disability and Rehabilitation, 2019
"Ehlers-Danlos syndrome" (EDS) is a heritable connective disorder influencing multiple aspects of daily life. Most studies have focused on describing the physical symptoms and level of disability, but little knowledge exists about the psychosocial effects of the pathology.
Stijn De Baets, Patrick Calders, Liesbeth Verhoost, Marieke Coussens, Inge Dewandele, Fransiska Malfait, Guy Vanderstraeten, Geert Van Hove, Dominique Van de Velde   +8 more
openaire   +3 more sources

Cardiovascular manifestations of hypermobile Ehlers–Danlos syndrome and hypermobility spectrum disorders

Vascular Medicine, 2022
Introduction: Mitral valve prolapse and aortic root dilatation are reported in association with hypermobile Ehlers–Danlos syndrome (hEDS), but the full phenotypic spectrum of cardiovascular complications in this condition has not been studied in the aftermath of updated nosology and diagnostic criteria.
Eman R Rashed, Tania Ruiz Maya, Jennifer Black, Veronica Fettig, Daniella Kadian-Dodov, Jeffrey W Olin, Lakshmi Mehta, Bruce D Gelb, Amy R Kontorovich   +8 more
openaire   +2 more sources

Benign Hypermobile Joint Syndrome and Ehlers-Danlos Syndrome

2004
Abstract Benign hypermobile joint syndrome is not really a disease at all. Instead, it is an inherited variation on normal. Children with benign hypermobile joint syndrome are often referred to as being double-jointed. Many children have loose joints or joints that they can voluntarily subluxate. The diagnosis of benign hypermobile joint
openaire   +1 more source

Hypermobile Ehlers-Danlos Syndrome and Hypermobility Spectrum Disorders.

American family physician, 2021
Hypermobile Ehlers-Danlos syndrome (EDS) and hypermobility spectrum disorders are the most common symptomatic joint hypermobility conditions seen in clinical practice. The 2017 International Classification of the Ehlers-Danlos syndromes replaced previous terms for symptomatic joint hypermobility with hypermobile EDS and introduced the term ...
Kenneth S, Yew, Kara A, Kamps-Schmitt, Robyn, Borge   +2 more
openaire   +3 more sources

Evidenzbasiert vorgehen – Hypermobiles Ehlers-Danlos-Syndrom

ergopraxis
Das hypermobile Ehlers-Danlos-Syndrom gehört zu den sogenannten seltenen Erkrankungen, die in der Ergotherapieausbildung oftmals wenig Beachtung finden. Umso interessanter erscheint die Frage, wie Ergotherapeut*innen in der Arbeit mit betroffenen Klient*innen evidenzbasiert vorgehen können.
openaire   +1 more source