A clinical case of Bruton agammaglobulinemia in a child of the RS (Ya)
https://doi.org/10.25789/YMJ.2019.68.34
Abstract
The article is devoted to the description of the clinical course of Bruton's disease in a child. Bruton's disease is a genetic disease associated with impaired synthesis of serum immunoglobulins and B cells. The disease belongs to the primary immunodeficiency.
About the Authors
O. N. IvanovaRussian Federation
Ivanova Olga Nikolaevna – MD, professor of Medical institute
677013, Ojunskogo 27, Yakutsk, Republic Sakha (Yakutia)
T. E. Burtseva
Russian Federation
Burtseva Tatyana Egorovna – MD, professor of the department of pediatrics and pediatric surgery, Medical institute
677013, Ojunskogo 27, Yakutsk, Republic Sakha (Yakutia);
a head of the laboratory
M. P. Slobodchikova
Russian Federation
Slobodchikova Maya Pavlovna – a senior lecturer of the department of foreign languages with the course of Russian and Latin languages
+7-911-908-7772
References
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Review
For citations:
Ivanova O.N., Burtseva T.E., Slobodchikova M.P. A clinical case of Bruton agammaglobulinemia in a child of the RS (Ya). Yakut Medical Journal. 2019;(4):122-123. https://doi.org/10.25789/YMJ.2019.68.34