Importance of biochemical markers in the diagnosis of congenital malformations of the fetus
https://doi.org/10.25694/URMJ.2018.03.011
Abstract
The study of diagnostic importance of biochemical screening of pregnant women on AFP and hCG for detection of congenital hereditary diseases was conducted. The main group consisted of 109 patients, in who congenital malformations and/or chromosomal anomalies of fetus or infant were diagnosed prenatally or after the birth. The control group consisted of 280 patients of RPC, whose pregnancy ended with the birth of children without congenital heredity diseases. The sufficiently high efficiency of detection in serum of blood AFP and hCG in the 2nd trimester of pregnancy during the formation of a risk group for congenital malformations (CM) and the chromosomal anomalies is shown in the article.
About the Authors
Z. U. Amaeva
ГБОУ ВПО «Дагестанская государственная медицинская академия» МЗ РФ
Russian Federation
Russian Federation
N. S.-M. Omarov
ГБОУ ВПО «Дагестанская государственная медицинская академия» МЗ РФ
Russian Federation
Russian Federation
D. K. Kantaeva
ГБОУ ВПО «Дагестанская государственная медицинская академия» МЗ РФ
Russian Federation
Russian Federation
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Review
For citations:
Amaeva ZU, Omarov NS, Kantaeva DK. Importance of biochemical markers in the diagnosis of congenital malformations of the fetus. Ural Medical Journal. 2018;(3):72-75. (In Russ.) https://doi.org/10.25694/URMJ.2018.03.011
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