FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS

This article analyzes the frequency of polymorphisms of hemostasis system and folate cycle protein genes associated with increased risk of thrombophilia based on the results of CHGMA (Chita State Medical Academy) genetic laboratory patients with reproductive health disorders. Method of research is a...

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Main Author: A. V. Markovsky
Format: Article
Language:Russian
Published: «REMEDIUM GROUP» Ltd. 2018-05-01
Series:Атеротромбоз
Subjects:
Online Access:https://www.aterotromboz.ru/jour/article/view/152
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author A. V. Markovsky
author_facet A. V. Markovsky
author_sort A. V. Markovsky
collection DOAJ
description This article analyzes the frequency of polymorphisms of hemostasis system and folate cycle protein genes associated with increased risk of thrombophilia based on the results of CHGMA (Chita State Medical Academy) genetic laboratory patients with reproductive health disorders. Method of research is allele-specific PCR. It was analyzed 1800 DNA samples. The most frequently mutations occur in the genes of receptors in the platelets and the folate cycle, mostly heterozygous substitution. Leiden mutation (F5) and prothrombin mutation (F2) are the most significant in the thrombophilia development and occur much less frequently. Only in one case revealed a homozygous mutation in the gene F2 and F5.
format Article
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institution OA Journals
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publisher «REMEDIUM GROUP» Ltd.
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series Атеротромбоз
spelling doaj-art-32cb2adaa3554dceacc172ce874372fe2025-08-20T02:17:41Zrus«REMEDIUM GROUP» Ltd.Атеротромбоз2307-11092658-59522018-05-0101707510.21518/2307-1109-2018-1-70-75134FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERSA. V. Markovsky0FSBI HPE «Chita State Medical Academy» of the Ministry of Healthcare of the Russion FederationThis article analyzes the frequency of polymorphisms of hemostasis system and folate cycle protein genes associated with increased risk of thrombophilia based on the results of CHGMA (Chita State Medical Academy) genetic laboratory patients with reproductive health disorders. Method of research is allele-specific PCR. It was analyzed 1800 DNA samples. The most frequently mutations occur in the genes of receptors in the platelets and the folate cycle, mostly heterozygous substitution. Leiden mutation (F5) and prothrombin mutation (F2) are the most significant in the thrombophilia development and occur much less frequently. Only in one case revealed a homozygous mutation in the gene F2 and F5.https://www.aterotromboz.ru/jour/article/view/152inherited thrombophiliahemostasis system genesfolate cycle protein genes
spellingShingle A. V. Markovsky
FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
Атеротромбоз
inherited thrombophilia
hemostasis system genes
folate cycle protein genes
title FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
title_full FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
title_fullStr FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
title_full_unstemmed FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
title_short FREQUENCY OF INHERITED THROMBOPHILIA GENE POLYMORPHISM IN WOMEN WITH REPRODUCTIVE HEALTH DISORDERS
title_sort frequency of inherited thrombophilia gene polymorphism in women with reproductive health disorders
topic inherited thrombophilia
hemostasis system genes
folate cycle protein genes
url https://www.aterotromboz.ru/jour/article/view/152
work_keys_str_mv AT avmarkovsky frequencyofinheritedthrombophiliagenepolymorphisminwomenwithreproductivehealthdisorders