Psoriasis vulgaris and autoimmune polyendocrine syndrome type I: a case report
Özet
Autoimmune polyglandular syndrome (APS) is a rarely diagnosed condition characterized by a combination of two or more organ-specific autoimmune diseases and divided into a very rare juvenile (APS type I) and a relatively common adult type (APS II-IV). The major components of APS-I are hypoparathyroidism, adrenal failure, and mucocutaneous candidiasis. In addition to the classic triad, many other autoimmune diseases could be associated with the syndrome. We report an adolescent patient with psoriasis vulgaris and APS-I.
Atıf için künye
Çayır, A., Engin, R. I., Turan, M. I., & Pala, E. (2014). Psoriasis vulgaris and autoimmune polyendocrine syndrome type I: a case report. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 27, 791–793. https://doi.org/10.1515/jpem-2013-0472
BibTeX
@article{cayir2014-239246,
author = {Çayır, Atilla and Engin, Ragip Ismail and Turan, Mehmet Ibrahim and Pala, Erdal},
title = {Psoriasis vulgaris and autoimmune polyendocrine syndrome type I: a case report},
journal = {JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM},
year = {2014},
volume = {27},
pages = {791--793},
issn = {0334-018X},
doi = {10.1515/jpem-2013-0472},
url = {https://akademik.atauni.edu.tr/yayinlar/239246-psoriasis-vulgaris-and-autoimmune-polyendocrine-syndrome-type-i-a-case-report}
}