Epidermólisis ampollosa congénita: Revisión del tema

C. Siañez-González, R. Pezoa-Jares, J. C. Salas-Alanis

Research output: Contribution to journalReview articlepeer-review

19 Citations (Scopus)

Abstract

Epidermolysis bullosa is a group of hereditary diseases affecting 1 in 17 000 live births worldwide. It consists of blistering of the skin and mucous membranes in response to minimal trauma. The disorder seriously affects the patient's quality of life. Diagnosis is based on immunofluorescence mapping and electron microscopy. Treatment is symptomatic, although new cellular and molecular therapies are currently under investigation. This review covers aspects of the molecular biology, clinical presentation, diagnosis, and treatment of epidermolysis bullosa relevant to improving the care for affected patients.
Original languageSpanish
Pages (from-to)842-856
Number of pages15
JournalActas Dermo-Sifiliograficas
Volume100
Issue number10
DOIs
Publication statusPublished - Dec 2009
Externally publishedYes

Bibliographical note

Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Histology
  • Dermatology

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