Epidermolysis bullosa simplex with muscular dystrophy. Review of the literature and a case report

BACKGROUND: Epidermolysis bullosa simplex associated with muscular dystrophy is a genetic skin disease caused by plectin deficiency. A case of a 19-year-old Czech patient affected with this disease and a review all previously published clinical cases are presented. MAIN OBSERVATIONS: In our patient,...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Dermatol Case Rep
Egile Nagusiak: Kyrova, Jana, Kopeckova, Lenka, Buckova, Hana, Mrazova, Lenka, Vesely, Karel, Hermanova, Marketa, Oslejskova, Hana, Fajkusova, Lenka
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Specjalisci Dermatolodzy 2016
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5385263/
https://ncbi.nlm.nih.gov/pubmed/28400893
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3315/jdcr.2016.1231
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