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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 

Annotation:

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)


1. Sozaeva L.S., Karmanov M.E., Breivik L. [et al.]. New immunological methods of diagnostics of an autoimmune poliglandulyar syndrome of 1 type (first experience in Russia) // Endocrinology Problems. 2015. No. 3. P. 4–8.
2. Orlova E.M. Genetic bases and clinical options of an autoimmune polyglandular syndrome of 1 type: Abstract of MD Thesis. Moscow, 2005. 22 p.
3. Fadeev V.V., Shevchenko U.V., Melnichenko G.A. Autoimmune poliglandulyar syndromes // Problems of Endocrinology. 1999. No. 1. P. 47–54.
4. Ahonen P. Autoimmune polyendocrinopathy – candidosis – ectodermal dystrophy (apeced): autosomal recessive inheritance // Clin. Genetic. 2008. Vol. 27, No. 6. Р. 535–542.

PUBLISHER: "MEDITSYNA DV"

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