Results 1 to 10 of about 1,081,004 (187)

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

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   +9 more sources

KLK15 alters connective tissues in hypermobile Ehlers-Danlos syndrome [PDF]

iScience
Summary: Hypermobile Ehlers-Danlos syndrome (hEDS) is a debilitating multisystem condition characterized by joint hypermobility, chronic pain, and diverse comorbidities, yet its genetic basis remains undefined.
Cortney Gensemer, Taylor Petrucci, Tyler Beck, Victoria Daylor, Molly Griggs, Charlotte Griggs, Amy Weintraub, Kathryn Byerly, Lilong Guo, Jordan Morningstar, Isabelle Kornblau, Rachel Biggs, Kelsey Moore, Natalie Koren, Christina Hastings, Emily Oberlies, Ella R. Zientara, Elsie Devey, Sarah Dooley, Kristina Stayer, Roman Fenner, Katherine Singleton, Sofia Luzbetak, Deatra Bear, Rebecca Byrd, Julianna Weninger, Erika Bistran, Gyda Beeson, Joshua Kerns, Madalyn Osterhaus, Emily Fleck, Jillian Schnaudigel, Shaina Butler, Sydney Severance, Wiley Kendall, Joe R. Delaney, Daniel P. Judge, Peng Chen, Hai Yao, Jan Guz, Alexander Awgulewitsch, Steven A. Kautz, Rupak Mukherjee, Robert Price, Fraser Henderson, Sr., Steven Shapiro, Clair A. Francomano, Jason C. Kovacic, Mark Lavallee, Amy R. Kontorovich, Takiy-Eddine Berrandou, Susan A. Slaugenhaupt, David Milan, Anne Maitland, Sunil Patel, Nabila Bouatia-Naji, Russell A. Norris   +56 more
doaj   +7 more sources

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

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

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

SAGE 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, Shannon Collins, Joshua St. Louis   +2 more
doaj   +3 more sources

Hypermobile Ehlers-Danlos Syndrome: Cerebrovascular, Autonomic and Neuropathic Features [PDF]

American Journal of Medicine Open
Background: Hypermobile Ehlers-Danlos syndrome (hEDS) affects multiple systems, but comprehensive evaluations of a larger sample of hEDS patients are lacking.
Peter Novak, MD, PhD, David M. Systrom, MD, Sadie P. Marciano, PA-C, Alexandra Witte, PA-C, Arabella Warren, MD, PhD, Donna Felsenstein, MD, Matthew P. Giannetti, MD, Matthew J. Hamilton, MD, Jennifer Nicoloro-SantaBarbara, PhD, Mariana Castells, MD, Khosro Farhad, MD, David M. Pilgrim, MD, William J. Mullally, MD, Mark C. Fishman, MD, Jeff M. Milunsky, MD, Aubrey Milunsky, MD, Joel Krier, MD   +16 more
doaj   +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

A case of massive hematoma: reflections on hypermobile Ehlers-Danlos syndrome [PDF]

Frontiers in Medicine
Ehlers-Danlos Syndrome (EDS) refers to a group of connective tissue disorders characterized by significant clinical and genetic variability, affecting multiple systems in the body. Classified as a rare disease, EDS includes 14 subtypes, all marked by joint hypermobility, skin extensibility, and tissue fragility. These subtypes present with a wide range
Liu Q, Zeng G, Xiong Y, Xu C.
exaly   +5 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   +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