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The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature
Anencephaly is a severe malformation of the central nervous system (CNS), being one of the most common types of neural tube defects. It is defined as total or partial absence of the calvarium, with absence of the brain. Anencephaly has an incidence of 1 to 5 in every 1000 births, and the mortality r...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864317/ https://www.ncbi.nlm.nih.gov/pubmed/33544785 http://dx.doi.org/10.47162/RJME.61.2.03 |
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author | Munteanu, Octavian Cîrstoiu, Monica Mihaela Filipoiu, Florin Mihail Neamţu, Maria Narcisa Stavarache, Irina Georgescu, Tiberiu Augustin Bratu, Ovidiu Gabriel Iorgulescu, Gabriela Bohîlţea, Roxana Elena |
author_facet | Munteanu, Octavian Cîrstoiu, Monica Mihaela Filipoiu, Florin Mihail Neamţu, Maria Narcisa Stavarache, Irina Georgescu, Tiberiu Augustin Bratu, Ovidiu Gabriel Iorgulescu, Gabriela Bohîlţea, Roxana Elena |
author_sort | Munteanu, Octavian |
collection | PubMed |
description | Anencephaly is a severe malformation of the central nervous system (CNS), being one of the most common types of neural tube defects. It is defined as total or partial absence of the calvarium, with absence of the brain. Anencephaly has an incidence of 1 to 5 in every 1000 births, and the mortality rate is 100% during intrauterine life or within hours or days after birth. The etiology of anencephaly remains unclear, but various maternal-related environmental and genetic risk factors have been reported, which include diabetes, obesity, exposure to different drugs or toxins, genetic polymorphisms and mutations, as well as positive family history for neural tube defects. One of the most important nutritional factors in the development of anencephaly is folate deficiency. Methylenetetrahydrofolate reductase (MTHFR) gene codes the enzyme involved in the intracellular metabolism of folic acid; the 677C-T polymorphism of this gene causes the thermolability of the enzyme and decreased enzymatic activity, which is also dependent of folate plasmatic level. Etiopathogenesis of anencephaly includes several mutations in various other genes, such as: platelet-derived growth factor receptor alpha (PDGFRA), cadherin epidermal growth factor (EGF) laminin G (LAG) seven-pass G-type receptor 1 (CELSR1), Vang-like 1 (VANGL1) and Vang-like 2 (VANGL2), the last two being involved in the process of neurulation. Screening tests include maternal serum alpha-fetoprotein level and ultrasound (US) examination. During the first trimester US screening, anencephaly is now detected in all cases, but in order to decrease the complication rate of pregnancy termination, the diagnosis should be established as soon as possible, during the pregnancy confirmation US. We conclude that given that anencephaly is a severe malformation of the CNS, morphological characterization could improve the screening by US that is mandatory in the first trimester in order to plan the best, safe and early management. |
format | Online Article Text |
id | pubmed-7864317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest |
record_format | MEDLINE/PubMed |
spelling | pubmed-78643172021-02-08 The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature Munteanu, Octavian Cîrstoiu, Monica Mihaela Filipoiu, Florin Mihail Neamţu, Maria Narcisa Stavarache, Irina Georgescu, Tiberiu Augustin Bratu, Ovidiu Gabriel Iorgulescu, Gabriela Bohîlţea, Roxana Elena Rom J Morphol Embryol Review Anencephaly is a severe malformation of the central nervous system (CNS), being one of the most common types of neural tube defects. It is defined as total or partial absence of the calvarium, with absence of the brain. Anencephaly has an incidence of 1 to 5 in every 1000 births, and the mortality rate is 100% during intrauterine life or within hours or days after birth. The etiology of anencephaly remains unclear, but various maternal-related environmental and genetic risk factors have been reported, which include diabetes, obesity, exposure to different drugs or toxins, genetic polymorphisms and mutations, as well as positive family history for neural tube defects. One of the most important nutritional factors in the development of anencephaly is folate deficiency. Methylenetetrahydrofolate reductase (MTHFR) gene codes the enzyme involved in the intracellular metabolism of folic acid; the 677C-T polymorphism of this gene causes the thermolability of the enzyme and decreased enzymatic activity, which is also dependent of folate plasmatic level. Etiopathogenesis of anencephaly includes several mutations in various other genes, such as: platelet-derived growth factor receptor alpha (PDGFRA), cadherin epidermal growth factor (EGF) laminin G (LAG) seven-pass G-type receptor 1 (CELSR1), Vang-like 1 (VANGL1) and Vang-like 2 (VANGL2), the last two being involved in the process of neurulation. Screening tests include maternal serum alpha-fetoprotein level and ultrasound (US) examination. During the first trimester US screening, anencephaly is now detected in all cases, but in order to decrease the complication rate of pregnancy termination, the diagnosis should be established as soon as possible, during the pregnancy confirmation US. We conclude that given that anencephaly is a severe malformation of the CNS, morphological characterization could improve the screening by US that is mandatory in the first trimester in order to plan the best, safe and early management. Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest 2020 2020-08-21 /pmc/articles/PMC7864317/ /pubmed/33544785 http://dx.doi.org/10.47162/RJME.61.2.03 Text en Copyright © 2020, Academy of Medical Sciences, Romanian Academy Publishing House, Bucharest http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited. |
spellingShingle | Review Munteanu, Octavian Cîrstoiu, Monica Mihaela Filipoiu, Florin Mihail Neamţu, Maria Narcisa Stavarache, Irina Georgescu, Tiberiu Augustin Bratu, Ovidiu Gabriel Iorgulescu, Gabriela Bohîlţea, Roxana Elena The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title | The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title_full | The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title_fullStr | The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title_full_unstemmed | The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title_short | The etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
title_sort | etiopathogenic and morphological spectrum of anencephaly: a comprehensive review of literature |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864317/ https://www.ncbi.nlm.nih.gov/pubmed/33544785 http://dx.doi.org/10.47162/RJME.61.2.03 |
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