FIELD: medicine.
SUBSTANCE: invention relates to medicine, namely to medical diagnostics, and can be used to predict the risk of developing low weight of newborns in unrelated Russian individuals, natives of the Central Chernozem region of the Russian Federation. DNA is isolated from peripheral venous blood. The polymorphic locus rs10496196 HK2, differentially expressed in the placenta, is analyzed. An increased risk of delivering babies with low body weight is predicted when the allele A of the polymorphic locus rs10496196 HK2 is detected.
EFFECT: method provides new criteria for assessing the risk of delivering low-birthweight babies in pregnant women of Russian nationality, natives of the Central Chernozem region of the Russian Federation, based on data on the polymorphic locus rs10496196 HK2.
1 cl, 1 tbl, 4 ex
| Title | Year | Author | Number |
|---|---|---|---|
| METHOD FOR PREDICTING THE WEIGHT OF A NEWBORN, TAKING INTO ACCOUNT GENETIC FACTORS | 2021 |
|
RU2775436C1 |
| METHOD FOR PREDICTING NEWBORN WEIGHT IN PREGNANT WOMEN WITH PREECLAMPSIA IN COMBINATION WITH FETAL GROWTH RETARDATION SYNDROME | 2020 |
|
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| METHOD FOR PREDICTING THE RISK OF FETAL GROWTH RETARDATION | 2021 |
|
RU2775435C1 |
| METHOD FOR PREDICTION OF NEWBORN'S WEIGHT BASED ON GENETIC DATA OF MOTHERS | 2023 |
|
RU2818358C1 |
| METHOD FOR PREDICTION OF NEWBORN'S WEIGHT IN PREGNANT WOMEN WITH PRE-ECLAMPSIA AND A FAMILY HISTORY OF PRE-ECLAMPSIA | 2020 |
|
RU2738685C1 |
| METHOD FOR PREDICTION OF NEWBORN'S WEIGHT TAKING INTO ACCOUNT POLYMORPHIC VERSION OF 10976 G/AFVII LOCUS | 2014 |
|
RU2557952C1 |
| METHOD FOR PREDICTING THE RISK OF FETAL GROWTH RETARDATION, TAKING INTO ACCOUNT EPISTATIC INTERACTIONS OF POLYMORPHIC MENARCHE LOCI | 2021 |
|
RU2775432C1 |
| METHOD FOR PREDICTING THE RISK OF DEVELOPING PREECLAMPSIA BASED ON MOLECULAR GENETIC ANALYSIS | 2021 |
|
RU2775433C1 |
| METHOD FOR PREDICTION OF GROWTH OF NEWBORNS USING DATA ON GENETIC POLYMORPHISM OF MOTHERS | 2023 |
|
RU2820498C1 |
| METHOD FOR PREDICTING THE RISK OF DEVELOPING FETAL GROWTH RETARDATION SYNDROME IN WOMEN WITH A BURDENED FAMILY HISTORY | 2021 |
|
RU2770869C1 |
