Results 1 to 10 of about 3,009 (151)

Phenotypic Clusters and Multimorbidity in Hypermobile Ehlers-Danlos Syndrome [PDF]

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   +4 more sources

Severe conjunctivochalasis in association with classic type Ehlers-Danlos syndrome [PDF]

BMC Ophthalmology, 2012
Background Inferior conjunctivochalasis is common, but is rarely severe enough to require conjunctival excision. This report describes a patient with severe conjunctivochalasis who was subsequently diagnosed with Ehlers Danlos Syndrome, Classic Type ...
Whitaker John K, Alexander Philip, Chau David YS, Tint Naing L   +3 more
doaj   +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   +2 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   +2 more sources

Cardiovascular, autonomic symptoms and quality of life in children with hypermobile Ehlers–Danlos syndrome [PDF]

SAGE Open Medicine
Objectives: Hypermobile Ehlers–Danlos syndrome is a connective tissue disorder characterized by joint hypermobility and other systemic manifestations. Cardiovascular, autonomic symptoms and dysautonomia are frequently reported in adults with hypermobile ...
Amanda K Hertel, William R Black, Ashley Lytch, Emily Cramer, Lindsey Malloy Walton, Jordan T Jones   +5 more
doaj   +2 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

Classification, nosology and diagnostics of Ehlers-Danlos syndrome [PDF]

Journal of Biomedicine and Translational Research, 2019
Ehlers-Danlos syndrome (EDS) comprises a group of heritable connective tissue disorders which has as cardinal features varying degrees of skin hyperextensibility, joint hypermobility, easy bruising and skin fragility.
Ben C J Hamel
doaj   +3 more sources

2-Chloroprocaine vs. Lidocaine in a Patient With Hypermobile Ehlers–Danlos Syndrome and a History of Local Anesthetic Resistance: A Case Report [PDF]

Case Reports in Anesthesiology
Patients with hypermobile Ehlers–Danlos syndrome (hEDS) have a higher reported prevalence of local anesthetic (LA) resistance and obstetric complications than the general population.
Jayanth Dasika, Zachary B. Deutch, Amie L. Hoefnagel   +2 more
doaj   +2 more sources

Hypermobile type Ehlers‐Danlos syndrome associated with hypogammaglobulinemia and fibromyalgia: A case‐based review on new classification, diagnosis, and multidisciplinary management

Clinical Case Reports, 2019
Key Clinical Message Hypermobile type Ehlers‐Danlos syndrome (hEDS) is an underdiagnosed connective tissue disorder characterized by generalized joint hypermobility, chronic fatigue, widespread joints pain, and impaired quality of life. Here, we reported
Wei Zhang, Kevin Windsor, Richard Jones, David Oscar Taunton   +3 more
doaj   +2 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   +2 more sources