Challenges of the differential diagnosis between the subtypes of the junctional epidermolysis bullosa: presentation of two clinical cases

Background: Epidermolysis bullosa (EB) is a rare hereditary skin disease. It is subdivided into EB simplex (EBS), junctional EB (JEB), dystrophic EB (DEB) and Kindler syndrome. JEB is diagnosed in 2 per 1,000,000 of the population. There are few descriptions of clinical JEB cases in the literature....

ver descrição completa

Detalhes bibliográficos

Principais autores:	Yu. Yu. Kotalevskaya, N. M. Marycheva
Formato:	Artigo
Idioma:	Russo
Publicado em:	MONIKI 2019-02-01
coleção:	Alʹmanah Kliničeskoj Mediciny
Assuntos:	junctional epidermolysis bullosa severe generalized junctional epidermolysis bullosa epidermolysis bullosa laryngo-onycho-cutaneous syndrome lama3 gene
Acesso em linha:	https://www.almclinmed.ru/jour/article/view/986
Tags:	Adicionar Tag Sem tags, seja o primeiro a adicionar uma tag!