Reproductive Health
In China, there are about 20-30 million birth defects per year. The total number of children with congenital disabilities is up to 60-120 million, accounting for about 4%-6% of the total number of births per year.The total incidence of neural tube malformation in China is high. How to effectively reduce the incidence of neural tube malformation is a hot spot of current research.
Product introduction
Folic acid (Folate) is a water-soluble B vitamins and a necessary vitamin for the synthesis of DNA. Folic acid is an indispensable substance for the manufacture of red blood cells, associated with vitamin B12 promoting the formation and maturation of red blood cells, and participates in the whole process of metabolism of the human body. The fluorescence PCR melting curve technique was used to detect the C677T and A1298C site of the MTHFR gene and the A66G site of the MTRR gene in the gene detection of folic acid metabolism.The genotypes were used to evaluate the ability of the individuals to utilizing the folic acid. Gene detection by folate metabolism can predict the absorption and utilization ability of folic acid among individuals, and help achieve guidances of personalized folic acid supplementation, which is of great significance for clinical medication.
Female folic acid deficiency and excessive harm
Folic acid deficiency During pregnancy, it is easy to cause fetal neural tube defects, congenital malformations, abortion and preeclampsia. The incidence of placental abruption is increased, resulting in the increase of homocysteine and the increase of risk of cardiovascular diseases such as stroke. | Folic acid overdose During pregnancy, zinc deficiency, aggravation of pregnancy reaction, increased incidence of childbirth complications, fetal acquired dysplasia, intelligence loss and immunity decrease, and increase the risk of colonic adenoma and breast cancer, leading to folate hypersensitivity. |
Related genes of folic acid
Detection significance
1. early prediction of the uptake and utilization of folic acid by different individuals, so as to screen out high risk people who are prone to folate deficiency.
2. the realization of individualized supplementation of folic acid, strengthening the compliance of folic acid, is of great significance to the guidance of clinical medication.
3. to strengthen prenatal screening and prenatal diagnosis for neural tube defects and to reduce the risk of birth defects.
Detection advantage
Detection process
Intended for
1. Early prediction of the ability of folic acid uptake and utilization for different individuals, so as to screen out high risk people who are prone to folate deficiency.
2. The realization of individualized supplementation of folic acid, strengthening the compliance of folic acid, is of great significance to the guidance of clinical medication.
3. To strengthen prenatal screening for neural tube defects and to reduce the risk of birth defects.
- Noninvasive prenatal gene detection
- Genetic testing for hereditary deafness
- Neonatal Genetic Metabolic Disease
- Chromosomal Abnormality
- Metabolic Capacity Of Folic Acid
- Detection of microdeletion of chromosome microdeletion
- Chromosome microarray (CMA)
- Detection of children's safety in drug use
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