The autoimmune polyglandular syndrome type 1 in children

Written by Shapkina L.A., Bocharnikova N.N.

  UDK: 616.45–97–056.7–053.2 | DOI: 10.17238/PmJ1609-1175.2019.1.91–93  Pages: 91–93 | Full text PDF | Open PDF 


The study describes a clinical observation of autoimmune polyglandular syndrome type 1 in a boy aged 11 y.o. The disease manifested a chronic adrenal insufficiency and symptoms of subclinical hypoparathyroidism. The diagnosis was confirmed after molecular and genetic test. Child’s condition became normal due to replacement therapy.

Links to authors:

L.A. Shapkina1, N.N. Bocharnikova2
1 Pacific State Medical University (2 Ostryakova Ave. Vladivostok 690002 Russian Federation),
2 Regional Clinical Hospital No. 2 (55 Russkaya St. Vladivostok 690050 Russian Federation)

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