Results 81 to 90 of about 1,012,341 (230)

[A case of Ehlers-Danlos syndrome].

open access: yesShoni shikagaku zasshi. The Japanese journal of pedodontics, 1989
Ehlers-Danlos syndrome, an inherited connective tissue disorder, is characterized by skin hyperextensibility, joint hypermobility and skin fragility. The disease is at least classified into 10 types, I to X, based on clinical features, biochemical abnormalities of the connective tissue and the mode of inheritance.
Seki, Mitsuko   +3 more
openaire   +2 more sources

Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings

open access: yesPeriodontology 2000, EarlyView.
AbstractPeriodontitis is a complex inflammatory disease in which the host genome, in conjunction with extrinsic factors, determines susceptibility and progression. Genetic predisposition is the strongest risk factor in the first decades of life. As people age, chronic exposure to the periodontal microbiome puts a strain on the proper maintenance of ...
Arne S. Schaefer   +4 more
wiley   +1 more source

Síndrome de Ehlers-Danlos e gravidez: relato de caso Ehlers-Danlos syndrome and pregnancy: a case report

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2003
A síndrome de Ehlers-Danlos é doença do tecido conjuntivo cuja associação com a gestação é extremamente rara, mas com complicações potencialmente fatais no ciclo gravídico-puerperal, como roturas vasculares e intestinais.
Marcelo Luís Nomura   +2 more
doaj   +1 more source

Understanding the Reproductive Life Planning Experiences of People With Disabilities in Ontario, Canada: A Qualitative Exploration

open access: yesPerspectives on Sexual and Reproductive Health, EarlyView.
ABSTRACT Introduction Reproductive life planning can be a valuable component of reproductive health promotion. However, little is known about attitudes, desires, and intentions regarding pregnancy among people with disabilities. This exploratory qualitative study aimed to understand the reproductive life planning experiences of women and gender‐diverse
Momina Khan   +3 more
wiley   +1 more source

Hypermobile Ehlers-Danlos Syndrome (hEDS) [PDF]

open access: yes, 2019
Ehlers-Danlos Syndrome is a genetic connective tissue disease with varying expressions and phenotypes. Hypermobile Ehlers-Danlos Syndrome (hEDS) is the most prevalent subgroup within this disease category.
Akers, Jocelyn
core  

Coronofrontal rhytidectomy: A new approach for the treatment of severe pseudoptosis and superior entropion in dogs

open access: yesVeterinary Ophthalmology, Volume 28, Issue 2, Page 403-412, March 2025.
Abstract Purpose To describe the use of coronofrontal rhytidectomy (CFR) for the treatment of severe pseudoptosis and superior entropion in dogs, and to provide guidelines for the selection of surgical technique depending on presentation. Methods A review of medical records of dogs that underwent rhytidectomy from 2002 to 2023 was carried out ...
Rita Vilao Cardoso   +5 more
wiley   +1 more source

Type V and type III collagen modulate the expression and assembly of fibronectin extracellar matrix in classic and vascular Ehlers-Danlos syndrome fibroblasts, affecting cell survival and migration

open access: yes, 2012
Extracellular matrix (ECM) regulates cell proliferation, migration, survival and gene expression, via signal transduction pathways differentially activated by ECM ligands interacting with specific integrins.
ZOPPI, Nicoletta   +2 more
core  

ORTHOPAEDIC ASPECTS OF THE EHLERS. DANLOS SYNDROME

open access: yes, 1969
1. The orthopaedic features of 100 patients with the Ehlers-Danlos syndrome are described. 2. The significance of these findings is discussed and comment is made of their relationship to the other stigmata of the syndrome.
F. Horan, P. Beighton
core   +1 more source

Carotid artery dissection linked to intermittent apnoeic swimming: A case–control study

open access: yesExperimental Physiology, EarlyView.
Abstract Internal carotid artery (ICA) dissection is a rare and potentially devastating cause of cerebral ischaemia, initiated by an intimal tear or rupture of the vasa vasorum, that can lead to an intraluminal thrombus, vascular stenosis, occlusion, or dissecting aneurysm formation.
Damian M. Bailey   +14 more
wiley   +1 more source

Ehlers-Danlos syndrome Type VI : Case report

open access: yes, 1998
Ehlers-Danlos sendromu bağ dokusunun genetik geçiş gösteren bir hastalığıdır. Burada, eklem gevşekliği, deri bulguları gibi sendromun temel bulgularının yanısıra belirgin kifoskolyozunun da olması nedeniyle Ehlers-Danlos tip VI tanısı almış, anne ve ...
Ferda Özkınay   +6 more
core  

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