Epidermólisis bulosa distrófica recesiva: Caso clínico

dc.creatorCordero M,Claudio
dc.creatorGonzález B,Sergio
dc.creatorCastillo A,Carmen
dc.creatorMorales C,Enrique
dc.creatorMisad S,Carlos
dc.creatorRuiz-Esquide E,Fernando
dc.date2004-05-01
dc.date.accessioned2017-03-07T15:32:11Z
dc.date.available2017-03-07T15:32:11Z
dc.identifierhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872004000500012
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/386868
dc.descriptionWe report a female newborn with a dystrophic epidermolysis bullosa. The diagnosis was made by electron microscopy of a bullous skin lesion. The importance of reaching a specific diagnosis is underscored. Close relatives can therefore be informed and educated about prognosis, etiology and the possibility of having new affected offspring. An accurate diagnosis can be reached through electronic microscopy or modern immunohistochemical techniques. Further complementary information given by conventional histology is required. A complete study is recommended to minimize errors in the intepretation of morphology (Rev Méd Chile 2004; 132: 614-8).
dc.formattext/html
dc.languagees
dc.publisherSociedad Médica de Santiago
dc.sourceRevista médica de Chile v.132 n.5 2004
dc.subjectEpidermolysis bullosa, dystrophica
dc.subjectSkin diseases, vesiculobullous
dc.titleEpidermólisis bulosa distrófica recesiva: Caso clínico
dc.typeArtículos de revistas


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