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A Case of Koebner Variant of Epidermolysis Bullosa Simplex
Journal of the Korean Society of Neonatology ; : 166-170, 2001.
Artículo en Coreano | WPRIM | ID: wpr-146414
ABSTRACT
Epidermolysis bullosa simplex (EBS), characterized by a cleavage plane through basal keratinocytes, is caused by a mutation of the genes encoding keratin 5 and 14. It is often regarded as the least severe form of Epidermolysis bullosa. In 1886, Koebner described the seasonal blisterings predominantly on the palms and soles but occurring on the other sites of friction with clothes as well. His name is often used to describe EBS with the generalized blisterings. We have experienced a case of Koebner variant of EBS in a two-day old male neonate whose father had the same EBS. Hereby, we report his clinical, histopathological findings with a brief review of the literature.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estaciones del Año / Queratinocitos / Epidermólisis Ampollosa Simple / Vesícula / Epidermólisis Ampollosa / Fricción / Queratina-5 / Padre Límite: Humanos / Masculino / Recién Nacido Idioma: Coreano Revista: Journal of the Korean Society of Neonatology Año: 2001 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Estaciones del Año / Queratinocitos / Epidermólisis Ampollosa Simple / Vesícula / Epidermólisis Ampollosa / Fricción / Queratina-5 / Padre Límite: Humanos / Masculino / Recién Nacido Idioma: Coreano Revista: Journal of the Korean Society of Neonatology Año: 2001 Tipo del documento: Artículo