Results 1 to 10 of about 1,247,077 (145)

Prevalence of Scoliosis in Hypermobile Ehlers-Danlos Syndrome [PDF]

European Medical Journal, 2021
Objective: The main purpose of this study was to evaluate the prevalence, form, and severity of scoliosis in a population of adults meeting the 2017 criteria for hypermobile Ehlers-Danlos syndrome (hEDS).
Fabrice Gillas, Ahmed Mekki, Malika Foy, Robert Carlier, Karelle Benistan   +4 more
doaj   +4 more sources

The Impact of Hypermobile “Ehlers-Danlos Syndrome” and Hypermobile Spectrum Disorder on Interpersonal Interactions and Relationships [PDF]

Frontiers in Rehabilitation Sciences, 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-
Stijn De Baets, Marieke De Temmerman, Patrick Calders, Fransiska Malfait, Geert Van Hove, Guy Vanderstraeten, Inge De Wandele, Inge De Wandele, Dominique Van de Velde   +8 more
doaj   +7 more sources

Prevalence of Hypermobile Ehlers-Danlos Syndrome in Postural Orthostatic Tachycardia Syndrome [PDF]

Autonomic Neuroscience: Basic and Clinical, 2020
Despite well-established clinical associations between Hypermobile Ehlers-Danlos syndrome (hEDS) and postural orthostatic tachycardia syndrome (POTS), the precise prevalence is unknown. We therefore evaluated for hEDS in 91 POTS participants using the 2017 hEDS diagnostic checklist, which has three major criteria: 1) generalized joint hypermobility ...
Rebecca Bascom, Howard Levy, Amy C Arnold   +2 more
exaly   +5 more sources

Gastrointestinal Symptoms in Marfan Syndrome and Hypermobile Ehlers-Danlos Syndrome [PDF]

Gastroenterology Research and Practice, 2018
Objective. Marfan syndrome (MS) is a multisystem disorder caused by a mutation in FBN1 gene. It shares some phenotypic features with hypermobile Ehlers-Danlos syndrome (EDS) such as joint hypermobility.
N. Inayet, J. O. Hayat, A. Kaul, M. Tome, A. Child, A. Poullis   +5 more
doaj   +6 more sources

Hypermobile Ehlers–Danlos Syndrome (a.k.a. Ehlers–Danlos Syndrome Type III and Ehlers–Danlos Syndrome Hypermobility Type): Clinical Description and Natural History [PDF]

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, 2017
The hypermobile type of Ehlers–Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissue. It has been described largely in those with musculoskeletal complaints including joint hypermobility, joint subluxations/dislocations, as well as skin and soft tissue manifestations.
Brad Tinkle, Marco Castori, Rodney Grahame   +2 more
exaly   +4 more sources

Phenotypic Clusters and Multimorbidity in Hypermobile Ehlers-Danlos Syndrome

Mayo Clinic Proceedings: Innovations, Quality & Outcomes
Objective: To perform a retrospective clinical study in order to investigate phenotypic penetrance within a large registry of patients with hypermobile Ehlers-Danlos syndrome (hEDS) to enhance diagnostic and treatment guidelines by understanding ...
Taylor Petrucci, BS, S. Jade Barclay, MPH, Cortney Gensemer, PhD, Jordan Morningstar, BS, Victoria Daylor, BFA, Kathryn Byerly, BS, Erika Bistran, BS, Molly Griggs, MEd, James M. Elliott, PhD, Teresa Kelechi, RN, PhD, Shannon Phillips, RN, PhD, Michelle Nichols, RN, PhD, Steven Shapiro, DMD, MD, Sunil Patel, MD, Nabila Bouatia-Naji, PhD, Russell A. Norris, PhD   +15 more
doaj   +5 more sources

Spontaneous Diaphragmatic Rupture in Hypermobile Type Ehlers-Danlos Syndrome [PDF]

Case Reports in Surgery, 2017
Ehlers-Danlos Syndrome refers to a spectrum of connective tissue disorders that have a variety of clinical manifestations. In this case, we present a spontaneous diaphragmatic rupture in a patient with type III Ehlers-Danlos Syndrome.
Ruchi Amin, Brett H. Waibel
doaj   +5 more sources

The Language of Pain in the Hypermobile Ehlers–Danlos Syndrome: Metaphors as a Key to Understanding the Experience of Pain and as a Rehabilitation Tool

Brain Sciences, 2023
Ehlers–Danlos syndromes are a heterogeneous group of Heritable Connective Tissue Disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility.
Filippo Camerota, Rachele Mariani, Giulia Cordiano, Michela Di Trani, Valentina Lodato, Alessandro Ferraris, Massimo Pasquini, Claudia Celletti   +7 more
doaj   +3 more sources

Cleidocranial dysplasia with hypermobile Ehlers-Danlos syndrome: A case report

Radiology Case Reports, 2023
Cleidocranial dysplasia (CCD) is a rare genetic skeletal syndrome. The most common features are open fontanelles, hypertelorism, mid-face retrusion, hypoplasia, or aplasia of the clavicles leading to excessive shoulder mobility, dental abnormalities such
Rengin Ibrahim, MSc, Omar Hamadah, PhD, Mahmoud Abdul-Hak, PhD, Aladdin Alshawa, MSc, Mohamad Alhasan Alouda, MSc   +4 more
doaj   +3 more sources

Comorbidity, misdiagnoses, and the diagnostic odyssey in patients with hypermobile Ehlers-Danlos syndrome

Genetics in Medicine Open, 2023
Purpose: The extent of comorbidity and misdiagnosis had been unclear for patients with hypermobile Ehlers-Danlos Syndrome (hEDS), a hereditary connective tissue disorder.
Colin M.E. Halverson, Sha Cao, Susan M. Perkins, Clair A. Francomano   +3 more
doaj   +3 more sources