Autoimmune polyglandular syndrome type I. Features of clinical manifestations, difficulties in diagnosis and methods of correction

Autoimmune polyglandular syndrome (APG) type I is an orphan disease with autosomal recessive inheritance caused by mutations in the autoimmune regulator gene (AIRE); the disease onset typically occurs in childhood. The disease is characterized by a wide variety of clinical manifestations with a cert...

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Autores principales:	G. A. Galkina, L. S. Mikhailichenko, D. I. Sozaeva, S. B. Berezhanskaya, A. A. Afonin
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	State Budget Educational Institute of Higher Professional Education, Rostov State Medical University, Ministry Health of Russian Federation 2021-12-01
Colección:	Медицинский вестник Юга России
Materias:	autoimmune polyglandular syndrome children adrenal insufficiency hypoparathyroidism hypocalcemia candidiasis
Acceso en línea:	https://www.medicalherald.ru/jour/article/view/1440
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