Data di Pubblicazione:
2016
Abstract:
Chronic mucocutaneous candidiasis (CMCC) is a heterogeneous group of disorders characterized by non-invasive persistent Candida species infections of the skin, nails, and mucous membranes. Heterozygous dominant gain-of-function (GOF) mutations in signal transducer and activator of transcription 1 (STAT1) have been described as causing impaired STAT1 dephosphorylation, diminished IL-17- producing T-cell numbers, and CMCC (1, 2). Here, we report on the case of a 17-year-old boy who presented to our Department for CMCC. He was born preterm (36 weeks) to healthy non-consanguineous parents from Italy, by a pregnancy complicated by threatened miscarriage and gestosis. This article is protected by copyright. All rights reserved.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Immunology and Allergy; Pediatrics, Perinatology and Child Health; Immunology
Elenco autori:
Giardino, Giuliana; Somma, Domenico; Cirillo, Emilia; Ruggiero, Giuseppina; Terrazzano, Giuseppe; Rubino, Valentina; Ursini, Matilde Valeria; Vairo, Donatella; Badolato, Raffaele; Carsetti, Rita; Leonardi, Antonio; Puel, Anne; Pignata, Claudio
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