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

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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Bibliographic Details
Main Authors: G. A. Galkina, L. S. Mikhailichenko, D. I. Sozaeva, S. B. Berezhanskaya, A. A. Afonin
Format: Article
Language:English
Published: State Budget Educational Institute of Higher Professional Education, Rostov State Medical University, Ministry Health of Russian Federation 2021-12-01
Series:Медицинский вестник Юга России
Subjects:
autoimmune polyglandular syndrome
children
adrenal insufficiency
hypoparathyroidism
hypocalcemia
candidiasis
Online Access:https://www.medicalherald.ru/jour/article/view/1440
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