Abstract
Neural tube defects (NTDs) are a group of diseases caused by a failure of closure of the neural tube. Its aetiology contains both environmental and genetic factors. NTDs have a polygenic background. Genes, which are linked with NTDs occurrence, are both directly and indirectly connected with controlling the process of closure of the neural tube. Ones of those are genes of metabolism of folic acid as MTHFR, MTR, MTRR, CBS, MTHFD, folic acid receptors (FR) regulator genes from PAX family, T, PDGFRA and BRCA1 genes.
MeSH terms
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / genetics
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase / metabolism
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Carrier Proteins / genetics
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Carrier Proteins / metabolism
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Cystathionine beta-Synthase / genetics
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Cystathionine beta-Synthase / metabolism
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Ferredoxin-NADP Reductase / genetics
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Ferredoxin-NADP Reductase / metabolism
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Folic Acid / metabolism*
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Genetic Predisposition to Disease
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Humans
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Methylenetetrahydrofolate Dehydrogenase (NADP) / genetics
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Methylenetetrahydrofolate Dehydrogenase (NADP) / metabolism
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Methylenetetrahydrofolate Reductase (NADPH2)
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Neural Tube Defects / enzymology*
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Neural Tube Defects / etiology
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Neural Tube Defects / genetics*
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Neural Tube Defects / prevention & control
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Oxidoreductases Acting on CH-NH Group Donors / genetics
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Risk Factors
Substances
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Carrier Proteins
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Folic Acid
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methionine synthase reductase
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Ferredoxin-NADP Reductase
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Oxidoreductases Acting on CH-NH Group Donors
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Methylenetetrahydrofolate Reductase (NADPH2)
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Methylenetetrahydrofolate Dehydrogenase (NADP)
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5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
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Cystathionine beta-Synthase