Results 101 to 110 of about 1,170,712 (223)

Ehlers–Danlos Syndrome: Not Just Joint Hypermobility

, 2018
Ehlers–Danlos syndrome is an umbrella term for a group of heritable soft connective tissue disorders which is characterized by joint hypermobility, skin texture and elasticity abnormalities, and visceral and vascular fragility or dysfunctions.
Tina Bregant, Milica Klopcic Spevak
core   +1 more source

Vascular-type Ehlers-Danlos syndrome caused by a hitherto unknown genetic mutation: a case report

Journal of Medical Case Reports, 2013
Introduction Vascular-type Ehlers-Danlos syndrome is an autosomal dominant disease that causes arterial spurting, intestinal perforation, uterine rupture and hemopneumothorax due to decreased production of type III collagen.
Kashizaki Fumihiro, Hatamochi Atsushi, Kamiya Kazunori, Yoshizu Akira, Okamoto Hiroaki   +4 more
doaj   +1 more source

EHLERS-DANLOS SYNDROME– AN OVERVIEW

International Journal of Biomedical and Advance Research, 2010
Ehlers-Danlos syndrome, hypermobility type is generally considered the least severe type of EDS, although significant complications, primarily musculoskeletal, can and do occur. The skin is often soft or velvety and may be mildly hyperextensible. Subluxations and dislocations are common; they may occur spontaneously or with minimal trauma and can be ...
openaire   +3 more sources

Vascular Ehlers-Danlos syndrome —All three coronary artery spontaneous dissections [PDF]

, 2009
SummaryVascular Ehlers-Danlos syndrome is an inherited connective-tissue disorder causing arterial and gastrointestinal fragility and spontaneous rupture of the large arteries, uterus, or bowel.
Ogasawara, Ken, Uejima, Tokuhisa, Oikawa, Yuji, Abe, Keiko, Yajima, Junji, Aizawa, Tadanori, Nakamura, Michinari   +6 more
core   +1 more source

A case of coexistence of Marfan and Ehlers-Danlos syndromes in a 15-year-old boy

, 2014
Marfan syndrome (MS) and Ehlers-Danlos syndrome (EDS) are examples of two rare genetic diseases characterized by disturbances in the structure of collagen.
Agnieszka Gazda, Zbigniew Swacha, Lidia Rutkowska-Sak   +2 more
core   +1 more source

Retrospective descriptive study of prevalence of symptoms of suspected connective tissue disease: focus on Ehlers-Danlos syndrome

openLo studio analizzerà la prevalenza di sintomi nella Sindrome di Ehlers Danlos cercando di descrivere eventuali sintomi maggiormente significativi per la ...
CALLEGARI, DAVIDE
core  

Ehlers-Danlos syndrome type IV

, 2007
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous ...
Germain Dominique P
core   +1 more source

Interdisciplinary pain rehabilitation for patients with Ehlers-Danlos syndrome and hypermobility spectrum disorders

Journal of Rehabilitation Medicine
Objective: Chronic pain is a common manifestation of Ehlers-Danlos syndrome and hypermobility spectrum disorders; thus it is often suggested that patients undergo generic interdisciplinary pain rehabilitation, despite there being little evidence to ...
Peter Molander, Mehmed Novo, Åsa Ringqvist, Andrea Hållstam, Hugo Hesser, Monika Löfgren, Britt-Marie Stålnacke, Björn Gerdle   +7 more
doaj   +1 more source

Ehlers-Danlos syndrome

The Journal of Pediatrics, 1999
P C, Rowe, D F, Barron, H, Calkins, I H, Maumenee, P Y, Tong, M T, Geraghty   +5 more
openaire   +2 more sources

Stroke in Ehlers-Danlos Syndrome Kyphoscoliotic Type: Dissection or Vasculitis?

, 2017
BACKGROUND: Patients with the kyphoscoliotic type of Ehlers-Danlos syndrome have an increased risk of vascular complications such as aortic dissection and perforation. Cerebral ischemia has only rarely been documented.
Martin Wiesmann, Martin Häusler, Kurth, Ingo, Häusler, Martin, Jalaie, Houman, Rohrbach, Marianne, Marianne Rohrbach, Houman Jalaie, Joachim Weis, Ingo Kurth, Weis, Joachim, Häusler, Martin Georg, Wiesmann, Martin, Quade, Annegret, Annegret Quade   +14 more
core   +1 more source