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Iniencephaly Clausus: A New Case With Clinical and Imaging Findings
Iniencephaly is a rare kind of neural tube defect that is classified into two types of iniencephaly apertus and iniencephaly clausus. This anomaly could be diagnosed prenatally by obstetric ultrasonography and terminated by therapeutic abortion; however, it could be undiagnosed until birth similar t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kowsar
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623770/ https://www.ncbi.nlm.nih.gov/pubmed/26528385 http://dx.doi.org/10.5812/iranjradiol.4790v2 |
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author | Khatami, Alireza Hasanzadeh, Mohsen Norouzi, Hedayat Esfandiari, Ehasn Mehrafarin, Mastooreh |
author_facet | Khatami, Alireza Hasanzadeh, Mohsen Norouzi, Hedayat Esfandiari, Ehasn Mehrafarin, Mastooreh |
author_sort | Khatami, Alireza |
collection | PubMed |
description | Iniencephaly is a rare kind of neural tube defect that is classified into two types of iniencephaly apertus and iniencephaly clausus. This anomaly could be diagnosed prenatally by obstetric ultrasonography and terminated by therapeutic abortion; however, it could be undiagnosed until birth similar to our case due to the abnormal position of the fetus or lack of experience of the sonographer. Due to abnormality of the neural tube, which causes abnormal head and neck position, all these cases will die shortly after birth. We hereby introduce the photos and imaging findings of a case of an alive neonate with iniencephaly clausus. |
format | Online Article Text |
id | pubmed-4623770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Kowsar |
record_format | MEDLINE/PubMed |
spelling | pubmed-46237702015-11-02 Iniencephaly Clausus: A New Case With Clinical and Imaging Findings Khatami, Alireza Hasanzadeh, Mohsen Norouzi, Hedayat Esfandiari, Ehasn Mehrafarin, Mastooreh Iran J Radiol Pediatric Imaging Iniencephaly is a rare kind of neural tube defect that is classified into two types of iniencephaly apertus and iniencephaly clausus. This anomaly could be diagnosed prenatally by obstetric ultrasonography and terminated by therapeutic abortion; however, it could be undiagnosed until birth similar to our case due to the abnormal position of the fetus or lack of experience of the sonographer. Due to abnormality of the neural tube, which causes abnormal head and neck position, all these cases will die shortly after birth. We hereby introduce the photos and imaging findings of a case of an alive neonate with iniencephaly clausus. Kowsar 2015-07-22 /pmc/articles/PMC4623770/ /pubmed/26528385 http://dx.doi.org/10.5812/iranjradiol.4790v2 Text en Copyright © 2015, Tehran University of Medical Sciences and Iranian Society of Radiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited. |
spellingShingle | Pediatric Imaging Khatami, Alireza Hasanzadeh, Mohsen Norouzi, Hedayat Esfandiari, Ehasn Mehrafarin, Mastooreh Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title | Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title_full | Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title_fullStr | Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title_full_unstemmed | Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title_short | Iniencephaly Clausus: A New Case With Clinical and Imaging Findings |
title_sort | iniencephaly clausus: a new case with clinical and imaging findings |
topic | Pediatric Imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4623770/ https://www.ncbi.nlm.nih.gov/pubmed/26528385 http://dx.doi.org/10.5812/iranjradiol.4790v2 |
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