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Neural tube defects: Different types and brief review of neurulation process and its clinical implication
Neural Tube Defects are the most typical congenital malformations, with almost 300,000 cases annually worldwide. The incidence varies amongst geographical ranges from 0.2 to up to 11 per 1000 live births. In India, incidence is reportedly higher in north than south and can be attributable to diet an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884297/ https://www.ncbi.nlm.nih.gov/pubmed/35280642 http://dx.doi.org/10.4103/jfmpc.jfmpc_904_21 |
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author | Ravi, Kumar S. Divasha, Hassan, Sameeullah B. Pasi, Rachna Mittra, Sangh Kumar, Raj |
author_facet | Ravi, Kumar S. Divasha, Hassan, Sameeullah B. Pasi, Rachna Mittra, Sangh Kumar, Raj |
author_sort | Ravi, Kumar S. |
collection | PubMed |
description | Neural Tube Defects are the most typical congenital malformations, with almost 300,000 cases annually worldwide. The incidence varies amongst geographical ranges from 0.2 to up to 11 per 1000 live births. In India, incidence is reportedly higher in north than south and can be attributable to diet and genetic variances. Etiology is multifactorial. Severe forms of whitethorn are allied with syndromes. Primary neurulation and secondary neurulation are the most crucial steps in the formation and closure of the neural tube; any interruption can lead to mild to severe NTDs depending on the level of insult during embryogenesis. Various molecular and cellular events take place simultaneously for neural tube bending and closure of the neural tube. Neurological deficit in the newborn is contingent on the level of defect and severity of the structures affected. Survival of the newborn also depends on the severity of the lesion. Folic acid supplementation in all prospective mothers, preferably 4 weeks before conception and at least 12 weeks after conception, can prevent NTDs in folic responsive groups. But there is a significant number of other causes leading to neural tube defects apart from folic acid. Hydrocephalus is the commonest abnormality allied with NTDs in syndromic cases. CONCLUSION: NTDs are a frequent cause of stillbirths, infant mortality, and palsies in children. There are various reasons for NTDs, but the process of neurulation points towards some factors of NTC, which can be taken care of to lessen the burden of NTDs. |
format | Online Article Text |
id | pubmed-8884297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-88842972022-03-10 Neural tube defects: Different types and brief review of neurulation process and its clinical implication Ravi, Kumar S. Divasha, Hassan, Sameeullah B. Pasi, Rachna Mittra, Sangh Kumar, Raj J Family Med Prim Care Review Article Neural Tube Defects are the most typical congenital malformations, with almost 300,000 cases annually worldwide. The incidence varies amongst geographical ranges from 0.2 to up to 11 per 1000 live births. In India, incidence is reportedly higher in north than south and can be attributable to diet and genetic variances. Etiology is multifactorial. Severe forms of whitethorn are allied with syndromes. Primary neurulation and secondary neurulation are the most crucial steps in the formation and closure of the neural tube; any interruption can lead to mild to severe NTDs depending on the level of insult during embryogenesis. Various molecular and cellular events take place simultaneously for neural tube bending and closure of the neural tube. Neurological deficit in the newborn is contingent on the level of defect and severity of the structures affected. Survival of the newborn also depends on the severity of the lesion. Folic acid supplementation in all prospective mothers, preferably 4 weeks before conception and at least 12 weeks after conception, can prevent NTDs in folic responsive groups. But there is a significant number of other causes leading to neural tube defects apart from folic acid. Hydrocephalus is the commonest abnormality allied with NTDs in syndromic cases. CONCLUSION: NTDs are a frequent cause of stillbirths, infant mortality, and palsies in children. There are various reasons for NTDs, but the process of neurulation points towards some factors of NTC, which can be taken care of to lessen the burden of NTDs. Wolters Kluwer - Medknow 2021-12 2021-12-27 /pmc/articles/PMC8884297/ /pubmed/35280642 http://dx.doi.org/10.4103/jfmpc.jfmpc_904_21 Text en Copyright: © 2021 Journal of Family Medicine and Primary Care https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Article Ravi, Kumar S. Divasha, Hassan, Sameeullah B. Pasi, Rachna Mittra, Sangh Kumar, Raj Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title | Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title_full | Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title_fullStr | Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title_full_unstemmed | Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title_short | Neural tube defects: Different types and brief review of neurulation process and its clinical implication |
title_sort | neural tube defects: different types and brief review of neurulation process and its clinical implication |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884297/ https://www.ncbi.nlm.nih.gov/pubmed/35280642 http://dx.doi.org/10.4103/jfmpc.jfmpc_904_21 |
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