Results 101 to 110 of about 3,078 (199)

Esophageal Striae as a Possible Gastrointestinal Manifestation of Hypermobile Ehlers-Danlos Syndrome. [PDF]

ACG Case Rep J
Eckardt AJ, Wehrmann T, Brueck CC.
europepmc   +3 more sources

The Complexities of Navigating the Healthcare System as an Autistic Individual with Ehlers-Danlos Syndrome: A Patient Perspective

Journal of Patient Experience
Autistic individuals with hypermobile Ehlers-Danlos syndrome (hEDS) often face unique challenges navigating healthcare systems due to lack of clinician awareness, diagnostic delays, misdiagnoses, and systemic barriers.
Sarah Clark
doaj   +1 more source

Multidisciplinary Approach to Treating Chronic Pain in Patients with Ehlers–Danlos Syndrome: Critically Appraised Topic

Journal of Pain Research, 2022
Kiley C Whalen, Wilson Crone Center for Physician Assistant Studies, Albany Medical College, Albany, NY, USACorrespondence: Wilson Crone, Center for Physician Assistant Studies, Albany Medical College, MC-4, 47 New Scotland Avenue, Albany, NY, 12208, USA,
Whalen KC, Crone W
doaj  

CORRELATION OF HYPERMOBILE EHLERS-DANLOS SYNDROME (EDS) AND THE JOINT DAMAGE ON DAILY LIFE OF AFFECTED PATIENTS: A BIBLIOGRAPHIC REVIEW [PDF]

Ehlers-Danlos Syndrome, known by the acronym EDS, is a genetic pathology that affects the synthesis of collagen, the main constituent protein connective tissue in the human body. Over the centuries, this pathology has been described several times, having
Amaral, Emanuelle Campos, Carvalho, Fernanda Almeida, Reis, Danilo Lemes, Reis, Dhayane Lemes, Silva, Samira Cordovil, Souza, Annie Kamilly Lima, Werneck, Luiza Vieira   +6 more
core   +2 more sources

Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome

Abstract Hypermobile Ehlers-Danlos syndrome (hEDS) is a common heritable connective tissue disorder that lacks a known genetic etiology. To identify genetic contributions to hEDS, whole exome sequencing was performed on families and a cohort of sporadic hEDS patients. A missense variant in Kallikrein-15 (KLK15 p.
Gensemer C, Beck T, Guo L, Petrucci T, Morningstar J, Kornblau I, Byerly K, Biggs R, Weintraub A, Moore K, Koren N, Daylor V, Hastings C, Oberlies E, Zientara ER, Devey E, Dooley S, Stayer K, Fenner R, Singleton K, Luzbetak S, Bear D, Byrd R, Weninger J, Bistran E, Beeson G, Kerns J, Griggs M, Griggs C, Osterhaus M, Fleck E, Schnaudigel J, Butler S, Severance S, Kendall W, Delaney JR, Judge DP, Chen P, Yao H, Guz J, Awgulewitsch A, Kautz SA, Mukherjee R, Price R, Henderson F, Shapiro S, Francomano CA, Kovacic JC, Lavallee M, Patel S, Berrandou T, Slaugenhaupt SA, Milan D, Kontorovich AR, Bouatia-Naji N, Norris RA.   +55 more
europepmc   +3 more sources

Surgical Treatment of the Glenohumeral Joint for Indications of Instability and Pain in Hypermobile Ehlers-Danlos Syndrome - Systematic Review

Quality in Sport
Introduction Ehlers-Danlos Syndrome (EDS) is a group of connective tissue disorders, the essence of which are abnormalities in the function of collagen. One type of EDS with an unknown genetic basis is the hypermobile form of EDS (hEDS).
Jędrzej Jabłoński, Filip Nadolny, Martyna Kania, Damian Grubski, Hanna Bartkowiak, Agnieszka Adamowska, Kacper Ziarnik, Alicja Śniatała   +7 more
doaj   +1 more source

An exploration of the journey to diagnosis of Ehlers-Danlos Syndrome (EDS) for women living in Australia [PDF]

IntroductionEhlers-Danlos syndromes (EDS) is an umbrella term for a group of hereditary connective tissue disorders usually featuring hyperextensible skin, easy bruising, poor healing, and joint hypermobility.
Flood, Terri, Trudgian, Rachel
core   +1 more source

THE CRITICAL ROLE OF EARLY DIAGNOSIS IN EHLERS-DANLOS SYNDROME: A COMPREHENSIVE REVIEW [PDF]

Introduction and purpose: Ehlers- Danlos syndrome (EDS) is a group of genetic connective tissue disorders with 13 distinguished subtypes. Approximately, 1 in 5000 people receive a diagnosis; however, this number is likely underestimated due to frequent ...
Aleksandra Borowy, Aleksandra Chajnowska, Barbara Wołoszyn, Julia Guzowska, Julia Stępień, Maciej Sobczyk, Małgorzata Zach, Patrycja Rzeźnik, Weronika Stachera, Wiktoria Suchcicka   +9 more
core   +2 more sources

Long COVID and hypermobility spectrum disorders have shared pathophysiology

Frontiers in Neurology
Hypermobility spectrum disorders (HSD) and hypermobile Ehlers–Danlos syndrome (hEDS) are the most common joint hypermobility conditions encountered by physicians, with hypermobile and classical EDS accounting for >90% of all cases.
Ravindra Ganesh, Bala Munipalli
doaj   +1 more source

An online pain management program for people with hypermobile Ehlers-Danlos Syndrome or hypermobility spectrum disorder : A three-staged development process [PDF]

Purpose Hypermobile Ehlers-Danlos Syndrome (hEDS) and hypermobility spectrum disorder (HSD) are painful, chronic and multi-systemic conditions. No online pain management programs for hEDS/HSD currently exist.
Chan, Cliffton, Chew, Min Tze, Ilhan, Emre, Kobayashi, Sarah, Nicholson, Leslie L.   +4 more
core   +1 more source