Association of the 677C→T Mutation on the Methylenetetrahydrofolate Reductase Gene in Turkish Patients With Neural Tube Defects
We report the analysis of the 677C→T mutation on the 5,10-methylenetetrahydrofolate reductase gene in Turkish controls and cases of neural tube defects. Mutation analysis of 91 patients with neural tube defects, 72 mothers, 63 fathers, and 93 healthy controls has been made by polymerase chain reacti...
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| Veröffentlicht in: | Journal of child neurology 1999-03, Vol.14 (3), p.159-161 |
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| creator | Boduroglu, Koray Alikaşifoğlu, Mehmet Anar, Burcu Tunçbilek, Ergul |
| description | We report the analysis of the 677C→T mutation on the 5,10-methylenetetrahydrofolate reductase gene in Turkish controls and cases of neural tube defects. Mutation analysis of 91 patients with neural tube defects, 72 mothers, 63 fathers, and 93 healthy controls has been made by polymerase chain reaction and allele specific restriction digestion with Hinf I. We did not find a significant difference in the 677C→T allele and genotype distribution among the patients with neural tube defects, their parents, and the control group. This result suggests that another mutation in the folate-related enzyme genes could be responsible for neural tube defects in Turkey. None of the mothers of patients with neural tube defects was advised to use folic acid as recommended to prevent neural tube defects. An immediate attempt to establish an education program for healthcare providers and women of childbearing age is crucial in Turkey. Furthermore, fortification of foods with folate would be a better approach. (J Child Neurol 1999;14:159-161). |
| doi_str_mv | 10.1177/088307389901400305 |
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Mutation analysis of 91 patients with neural tube defects, 72 mothers, 63 fathers, and 93 healthy controls has been made by polymerase chain reaction and allele specific restriction digestion with Hinf I. We did not find a significant difference in the 677C→T allele and genotype distribution among the patients with neural tube defects, their parents, and the control group. This result suggests that another mutation in the folate-related enzyme genes could be responsible for neural tube defects in Turkey. None of the mothers of patients with neural tube defects was advised to use folic acid as recommended to prevent neural tube defects. An immediate attempt to establish an education program for healthcare providers and women of childbearing age is crucial in Turkey. Furthermore, fortification of foods with folate would be a better approach. 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Mutation analysis of 91 patients with neural tube defects, 72 mothers, 63 fathers, and 93 healthy controls has been made by polymerase chain reaction and allele specific restriction digestion with Hinf I. We did not find a significant difference in the 677C→T allele and genotype distribution among the patients with neural tube defects, their parents, and the control group. This result suggests that another mutation in the folate-related enzyme genes could be responsible for neural tube defects in Turkey. None of the mothers of patients with neural tube defects was advised to use folic acid as recommended to prevent neural tube defects. An immediate attempt to establish an education program for healthcare providers and women of childbearing age is crucial in Turkey. Furthermore, fortification of foods with folate would be a better approach. (J Child Neurol 1999;14:159-161).</description><subject>Adult</subject><subject>Alleles</subject><subject>Female</subject><subject>Folic Acid - therapeutic use</subject><subject>Genetic Predisposition to Disease - genetics</subject><subject>Genetic Testing</subject><subject>Genotype</subject><subject>Homocysteine - genetics</subject><subject>Homocysteine - metabolism</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Methylenetetrahydrofolate Reductase (NADPH2)</subject><subject>Mutation - genetics</subject><subject>Neural Tube Defects - epidemiology</subject><subject>Neural Tube Defects - genetics</subject><subject>Neural Tube Defects - prevention & control</subject><subject>Oxidoreductases Acting on CH-NH Group Donors - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Turkey - epidemiology</subject><issn>0883-0738</issn><issn>1708-8283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kcFu1DAQhi0EokvhBTggiwO3tGM7ie1jtUBBailCizhGXntMUrJxazuHPXLhAXhEngRvdyUQlTiNNP83_8zoJ-Q5gxPGpDwFpQRIobQGVgMIaB6QBZOgKsWVeEgWO6DaEUfkSUrXAKAaDY_JEQOmgbftgnw_SynYweQhTDR4mnukrZTLXz9-rujlnA_CdCdcYu63I06YMUfTb10MPowmI_2EbrbZJKTnRabDRFdz_Daknn4sDjjlRL8MuacfcI5mLOIa6Wv0aHN6Sh55MyZ8dqjH5PPbN6vlu-ri6vz98uyisqJtcyXBc_DWguZ1o7FxgtsGHJSG9lZ45jzoGrRac6GUawVKcJxJV4t6XXsjjsmrve9NDLczptxthmRxHM2EYU5dq9vyOPACvvwHvA5znMptHecgGiYYKxDfQzaGlCL67iYOGxO3HYNul053P50y9OLgPK836P4a2cdRgNM9kMxX_LP2P5a_AY0rmCI</recordid><startdate>19990301</startdate><enddate>19990301</enddate><creator>Boduroglu, Koray</creator><creator>Alikaşifoğlu, Mehmet</creator><creator>Anar, Burcu</creator><creator>Tunçbilek, Ergul</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88B</scope><scope>88E</scope><scope>88G</scope><scope>8A4</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M3G</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>19990301</creationdate><title>Association of the 677C→T Mutation on the Methylenetetrahydrofolate Reductase Gene in Turkish Patients With Neural Tube Defects</title><author>Boduroglu, Koray ; 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Mutation analysis of 91 patients with neural tube defects, 72 mothers, 63 fathers, and 93 healthy controls has been made by polymerase chain reaction and allele specific restriction digestion with Hinf I. We did not find a significant difference in the 677C→T allele and genotype distribution among the patients with neural tube defects, their parents, and the control group. This result suggests that another mutation in the folate-related enzyme genes could be responsible for neural tube defects in Turkey. None of the mothers of patients with neural tube defects was advised to use folic acid as recommended to prevent neural tube defects. An immediate attempt to establish an education program for healthcare providers and women of childbearing age is crucial in Turkey. Furthermore, fortification of foods with folate would be a better approach. (J Child Neurol 1999;14:159-161).</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>10190266</pmid><doi>10.1177/088307389901400305</doi><tpages>3</tpages></addata></record> |
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| ispartof | Journal of child neurology, 1999-03, Vol.14 (3), p.159-161 |
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| source | SAGE Complete A-Z List; MEDLINE |
| subjects | Adult Alleles Female Folic Acid - therapeutic use Genetic Predisposition to Disease - genetics Genetic Testing Genotype Homocysteine - genetics Homocysteine - metabolism Humans Infant Infant, Newborn Male Methylenetetrahydrofolate Reductase (NADPH2) Mutation - genetics Neural Tube Defects - epidemiology Neural Tube Defects - genetics Neural Tube Defects - prevention & control Oxidoreductases Acting on CH-NH Group Donors - genetics Polymerase Chain Reaction Turkey - epidemiology |
| title | Association of the 677C→T Mutation on the Methylenetetrahydrofolate Reductase Gene in Turkish Patients With Neural Tube Defects |
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