Cutaneous vasculitis in patients with autoimmune polyendocrine syndrome type 1: report of a case and brief review of the literature

BACKGROUND: Autoimmune polyendocrine syndrome type 1, also known as autoimmune polyendocrinopathy-candidiasis-ectodermal-dystrophy, is a rare autosomal recessive disease due to pathogenic variants in the AIRE gene. Classic features of the syndrome are mucocutaneous candidiasis, chronic idiopathic hy...

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Vydáno v:BMC Pediatr
Hlavní autoři: Improda, Nicola, Capalbo, Donatella, Cirillo, Emilia, Cerbone, Manuela, Esposito, Andrea, Pignata, Claudio, Salerno, Mariacarolina
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2014
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4286916/
https://ncbi.nlm.nih.gov/pubmed/25361846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-14-272
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