Results 101 to 110 of about 1,279,374 (224)

Ehlers-Danlos syndrome associated with acute pancreatitis [PDF]

, 1989
The Ehlers-Danlos syndrome is a polysystemic inherited connective tissue disease characterized by articular laxity, hyperelastic skin, a tendency to excessive bleeding in the presence of minimal trauma, and friability of different tissues.
Jimenez,, Sarra-Carbonell,
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Walsh & Hoyt: Ehlers-Danlos Syndrome, Marafan\u27s Syndrome, and Pseudoxanthoma Elasticum

, 2005
Ehlers-Danlos syndrome encompasses a group of inherited disorders of connective tissue, all of which have abnormalities of collagen ...
Steven A. Newman, MD
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Ehlers-Danlos Sendromu

, 2021
Ehlers-Danlos Syndrome (EDS) is a heterogeneous group of inherited diseases with jointhypermobility, skin hyperextensibility and tissue fragility. There is no specific treatment for EDS.
Giray Bozkaya, Özlem
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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 and neurological features: a review

, 2011
Ehlers-Danlos Syndrome is a term that comprises a variety of inherited connective tissue disorders characterized primarily by skin hyperextensibility, joints hypermobility and excessive dislocations, easy bruisability, generalized fragility.
Merli P, Savasta S, Bianchi L, Ruggieri M, Spartà MV   +4 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
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Familial gigantiform cementoma with Ehlers- Danlos syndrome: A report of 2 cases

, 2015
Ehlers-Danlos syndrome is an autosomal dominant hereditary disorder of connective tissue, while familial gigantiform cementoma is a condition that usually manifests as multiple radiopaque cementum-like masses throughout the jaws.
Olcay Şakar, Sakar, Olcay, Unalan, Fatma, Aksakalli, Nihan, Mumcu, Zeynep, Fatma Ünalan, Aren, Gamze, Tolgay, Ceren Guney, Gamze Aren, Nihan Aksakallı, Ceren Güney Tolgay, Zeynep Mumcu   +11 more
core   +1 more source

Spontaneous Carotid-Cavernous Fistula in Ehlers Danlos Syndrome

, 2023
Spontaneous direct carotid-cavernous fistula (CCF) in young patients should prompt consideration for underlying connective tissue disease namely: Ehlers Danlos syndrome (EDS), peudoxanthoma elasticum (PXE), Marfan Syndrome, Loeys-Dietz syndrome and ...
Su Ann Lim; Saumya Jamuar; Saravana Kumar; Wickly Lee; Breana Cham; Julian Han; Hnin Hnin Oo
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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– 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