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2013 | 8 | 6 | 707-712
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Maternal factors and associated anomalies in NTD fetuses from Tunisia

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1 - 12 - 2013
6 - 12 - 2013
  • Department of Anatomy, Histology and Embryology, Medical University — Plovdiv, Plovdiv, 4000, 15A Vassil Aprilov Street, Bulgaria
  • Faculty of Biology, University of Plovdiv “Paisii Hilendarski”, Plovdiv, 4000, 24 Tsar Asen Street, Bulgaria
  • Department of Fetopathology and Embryology, Center of Maternity and Neonatology, Tunis, 1007, Rabta, Tunisia
  • Department of Fetopathology and Embryology, Center of Maternity and Neonatology, Tunis, 1007, Rabta, Tunisia
  • [1] Dolk H., Loane M., Garne E. The prevalence of congenital anomalies in Europe. Adv Exp Med Biol, 2010, 686, 349–364[Crossref]
  • [2] Henk J. Folic acid, methylation and neural tube closure in humans. Birth Defects Res., 2009, 85, 295–302[Crossref]
  • [3] Lindenbaum J., Savage D.G., Stabler S.P., Allen R.H. Diagnosis of cobalamin deficiency: relative sensitivities of serum cobalamin. Methylmalonic acid and total homocysteine concentrations. Am J Hem., 1990, 34, 99–107[Crossref]
  • [4] Seyit C.T., Beyan C., Atay V., Yaman H., Alanbay I., Kaptan A. Serum vitamin B12 and homocysteine levels in pregnant women with neural tube defect. Gynecological Endocrinology, 2010, 26, 578–581[WoS]
  • [5] Stonek F., Hafner E., Philipp K., Hefler L.A., Bentz E.K., Tempfer C.B. Methylenetetrahydrofolate reductase C677T polymorphism and pregnancy complications. Obstet Gynecol., 2007, 110, 363–368[WoS][Crossref]
  • [6] Koch M.C., Stegmann K., Ziegler A., Schröter B., Ermert A. Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population. Eur J Pediatr., 1998, 157, 487–492[Crossref]
  • [7] Mornet E., Muller F., Lenvoisé-Furet A., Delezoide A.L., Col J.Y., Simon-Bouy B. Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects. Hum Genet, 1997, 100, 512–514[Crossref]
  • [8] Weitkamp L.R., Tackels D.C., Hunter A.G., Holmes L.B., Schwartz C.E. Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives. Lancet, 1998, 1554–1555 [PubMed]
  • [9] Martínez-Villarreal L.E., Delgado-Enciso I., Valdéz-Leal R., Ortíz-López R., Rojas-Martínez A., Limón-Benavides C. Folate levels and N(5), N(10) - methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a casecontrol study. Arch Med Res., 2001, 32, 277–282[Crossref]
  • [10] Al-Gazali L.I, Padmanabhan R., Melnyk S., Yi P., Pogribny I.P., Pogribna M. Abnormal folate metabolism and genetic polymorphism of the folate path way in a child with Down syndrome and neural tube defect. Am J Med Genet, 2001, 103, 128–132[Crossref]
  • [11] Doğan H., Sahinoglu S. Fetuses with neural tube defects: ethical approaches and the role of health care professionals in Turkish health care institutions. Nurs Ethics., 2005, 12, 59–78[Crossref]
  • [12] Onrat S.T., Seyman H., Konuk M. Incidence of neural tube defects in Afyonkarahisar, Western Turkey. Genet Mol Res., 2009, 8, 154–156[Crossref]
  • [13] Golalipour M.J., Mobasheri E., Vakili M.A., Keshtkar A.A. Epidemiology of neural tube defects in northern Iran, 1998–2003. East Mediterr Health J., 2007, 13, 560–566
  • [14] Golalipour M.J, Najafi L., Keshtkar AA. Neural Tube Defects in Native Fars Ethnicity in Northern Iran. Iranian Journal Of Public Health, 2010, 3, 116–123
  • [15] Afshar M., Golalipour M.J., Farhud D. Epidemiologic aspects of neural tube defects in South East Iran Neurosciences, 2006, 11, 289–292
  • [16] Behrooz A. Prevalence of neural tube defect and its relative factors in south-west of Iran. Pakistan Journal Of Medical Sciences, 2007, 23, 654–656
  • [17] Al-Ani Z.R., Al-Hiali S.J., Al-Mehimdi S.M. Neural tube defects among neonates delivered in Al-Ramadi Maternity and Children’s Hospital, western Iraq. Saudi Med J., 2010, 31, 163–169
  • [18] Houcher B., Bourouba R., Djabi F., Houcher Z. The prevalence of neural tube defects in Setif University Maternity Hospital, Algeria-3 years review (2004–2006). Pteridines, 2008, 19, 12–18[Crossref]
  • [19] De la Vega A., López-Cepero R. Seasonal variations in the incidence of some congenital anomalies in Puerto Rico based on the timing of conception. P R Health Sci J., 2009, 28, 121–125
  • [20] Siffel C., Alverson C.J., Correa A. Analysis of seasonal variation of birth defects in Atlanta. Birth Defects Res A Clin Mol Teratol., 2005,73,655–662[Crossref]
  • [21] Perveen F., Tyyab S. Frequency and pattern of distribution of congenital anomalies in the newborn and associated maternal risk factors. J Coll Physicians Surg Pak., 2007, 17, 340–343 [PubMed]
  • [22] Sreenivas T., Nataraj A.R. Parental consanguinity and associated factors in congenital talipes equinovarus. Foot, 2012, 1, 2–5[Crossref]
  • [23] Abd E., Ghani A., El Ansarry K. Neural Tube Defects. Asjog., 2006, 3. Available from: URL: Accessed November 12, 2010
  • [24] Dias M.S., Partington M. Embryology of myelomeningocele and anencephaly. Neurosurg Focus, 2004,16, E1[Crossref]
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