Inherited epidermolysis bullosa: clinical and therapeutic aspects

Inherited epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders that present with skin and, in some cases, mucosal fragility, predisposing patients to the development of blisters and/or erosions after minimal trauma or friction. Children with a recurrent history of these kinds of lesions or neonates that present them in the absence of another reasonable explanation should be investigated. Diagnosis must be based on clinical and histopathological findings. To date, management of inherited EB basically consists in avoiding traumas that trigger lesions, as well as preventing infection and facilitating healing of the wounds with the systematic use of bandages.

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Bibliographic Details
Main Authors: Boeira,Vanessa Lys Simas Yamakawa, Souza,Erica Sales, Rocha,Bruno de Oliveira, Oliveira,Pedro Dantas, Oliveira,Maria de Fátima Santos Paim de, Rêgo,Vitória Regina Pedreira de Almeida, Follador,Ivonise
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Dermatologia 2013
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0365-05962013000200185
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