Results 21 to 30 of about 1,081,004 (187)

Hypoglycemia Associated With Hypermobile Ehlers-Danlos Syndrome. [PDF]

JCEM Case Rep
Abstract Hypoglycemia in the absence of diabetes is often multifactorial and challenging to diagnose definitively. We present a case report and an expanded series of adult females with reactive hypoglycemia who were diagnosed with Ehlers-Danlos syndrome (EDS).
Saeed H, Sheehan A, Patti ME.
europepmc   +3 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   +4 more sources

Web-based survey investigating cardiovascular complications in hypermobile Ehlers-Danlos syndrome after COVID-19 infection and vaccination.

PLoS ONE
BackgroundHypermobile Ehlers-Danlos syndrome is a heritable connective tissue disorder associated with generalized joint hypermobility but also other multisystem comorbidities, many of which may be exacerbated during a viral illness or after a ...
Anthony L Guerrerio, Allyson Mateja, Gretchen MacCarrick, Jonathan Fintzi, Erica Brittain, Pamela A Frischmeyer-Guerrerio, Harry C Dietz   +6 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

Application of immunotherapy for neurological manifestations in hypermobile Ehlers–Danlos syndrome [PDF]

Therapeutic Advances in Neurological Disorders, 2018
Ehlers–Danlos syndrome (EDS) is a heterogeneous heritable connective tissue disorder with various neurological manifestations, including chronic pain.
Manabu Araki, Youwei Lin, Hirohiko Ono, Wakiro Sato, Takashi Yamamura   +4 more
doaj   +3 more sources

Change in gliding properties of the iliotibial tract in hypermobile Ehlers–Danlos Syndrome [PDF]

Journal of Ultrasound, 2023
Abstract Purpose Fascial changes in hypermobile Ehlers–Danlos syndrome (hEDS), a heritable connective tissue disorder, can be used visualized with sonoelastography. The purpose of this study was to explore the inter-fascial gliding characteristics in hEDS.
Tina J. Wang, Antonio Stecco, Robert Schleip, Carla Stecco, Carmelo Pirri   +4 more
openaire   +4 more sources

Insomnia due to a dislocation storm in hypermobile Ehlers-Danlos syndrome with small fibre neuropathy and recurrent syncope [PDF]

European Journal of Translational Myology
Objective: To report on a patient with hypermobile Ehlers-Danlos syndrome (EDS) with SFN in whom frequent dislocations during sleep led to sleep deprivation. Case report: The patient is a 19-year-old female with hypermobile EDS manifested by frequent
Josef Finsterer
doaj   +2 more sources

Social media use by patients with hypermobile Ehlers–Danlos syndrome

Molecular Genetics & Genomic Medicine
Background Patients with uncommon genetic conditions often face limited in‐person resources for social and informational support. Hypermobile Ehlers–Danlos syndrome (hEDS) is a rare or underdiagnosed hereditary disorder of the connective tissue, and like
Colin M. E. Halverson, Tom A. Doyle, Samantha Vershaw   +2 more
doaj   +3 more sources

Cesarean Delivery in a Patient With Hypermobile Ehlers-Danlos Syndrome: A Case Report. [PDF]

Cureus
Patients with hypermobile Ehlers-Danlos syndrome (hEDS) usually present with generalized joint hypermobility and pain, soft and hyperextensible skin with atrophic scars and easy bruising, periodontitis, mitral valve prolapse, and aortic root dilation.
Antunes B, Araújo M, Noversa C, Pedreira J, Marques M.   +4 more
europepmc   +3 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   +4 more sources