Evolución clínica de la Epidermiosis Bullosa Neonatal en el Servicio de Neonatología Hospital para el Niño IMIEM [PDF]
, 2014 La epidermélisis bullosa engloba un grupo de enfermedades hereditarias que afectan a uno de cada 17,000 nacidos vivos en el mundo. Consiste en la formación de ampollas ante el menor traumatismo que afectan a la piel y a las mucosas.
García Robledo, Juan Fernando +1 more
core
Management of epidermolysis bullosa simplex in pregnancy: A case report
Case Reports in Women's Health, 2019 Epidermolysis bullosa (EB) encompasses a group of diseases characterized by extreme fragility of skin and mucous membranes, resulting in blister formation following minimal injury.
Nidhi Shah +2 more
doaj +1 more source
Periodontology 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
Modern methods of the treatment of hereditary epidermolysis bullosa
Vestnik Dermatologii i Venerologii, 2017 Today there are no ethiopathogenetic treatment methods for treating hereditary epidermolysis bullosa. All available treatment methods are symptomatic and are mainly aimed at patient care.
A. A. Kubanov +3 more
doaj +1 more source
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients. [PDF]
, 2019 BACKGROUND: Kindler Syndrome (KS) is a rare genodermatosis characterized by skin fragility, skin atrophy, premature aging and poikiloderma. It is caused by mutations in the FERMT1 gene, which encodes kindlin-1, a protein involved in integrin signalling ...
Castiglia, Daniele +14 more
core +3 more sources
استفاده از پردة آمنیون در درمان کنتراکچرهای دست در بیماران مبتلا به اپیدرمولیزیس بولوزا [PDF]
, 2008 زمینه و هدف: بیماران مبتلا به اپیدرمولیزیس بولوزا (Epidermolysis Bullsa [EB]) در طول دوران حیات خود با عوارض متعددی مواجه خواهند بود که یکی از این عوارض کنتراکچرهای دست میباشد که متأسفـانه تاکنون درمان موفقی نداشته است.
جعفريمنصوري, مريم +3 more
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Dental implants in patients with oral mucosal alterations : an update [PDF]
, 2011 Objective: To determine whether a series of diseases of the oral mucosa - Sjögren syndrome, ectodermal dysplasia, epidermolysis bullosa and lichen planus - reduce the survival rate of dental implants. Material and Method: A Medline search was carried out
Ata-Ali Mahmud, Francisco Javier +4 more
core +1 more source
The puzzling effect of disease severity on quality of life in epidermolysis bullosa
Journal of the European Academy of Dermatology and Venereology, EarlyView.
Vinzenz Hübl +4 more
wiley +1 more source
BMC Research Notes / Urine is a novel source of autologous mesenchymal stem cells for patients with epidermolysis bullosa [PDF]
, 2015 Background: Regenerative medicine is strictly dependent on stem cells as a source for a high diversity of somatic cells. However, the isolation of such from individuals suffering from severe genetic skin blistering diseases like epidermolysis bullosa (EB)
Bauer, Johann W. +9 more
core +1 more source
Junctional Epidermolysis Bullosa
Journal of the Chinese Medical Association, 2006 Epidermolysis bullosa (EB) encompasses a heterogeneous group of genodermatoses, characterized by fragility and blistering of the skin, often associated with extracutaneous manifestations. The level of vesiculation within the skin defines 3 major subtypes of EB: EB simplex, junctional EB, and dystrophic EB.
Kao, Chuan-Hong +5 more
openaire +2 more sources