Late-onset autoimmune polyendocrine syndrome type 1: a case report and literature review

Autoimmune polyendocrine syndrome type 1 (APS-1), also referred to as autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), a rare monogenic disorder, is classically characterized by a triad of chronic mucocutaneous candidiasis, hypoparathyroidism, and primary adrenal insufficienc...

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Detalles Bibliográficos
Autores principales: Zhan, Feixia, Cao, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889704/
https://www.ncbi.nlm.nih.gov/pubmed/33599910
http://dx.doi.org/10.1007/s12026-021-09180-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889704/
https://www.ncbi.nlm.nih.gov/pubmed/33599910
http://dx.doi.org/10.1007/s12026-021-09180-w

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