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Iniencephaly clausus: A case report with review of literature

Iniencephaly is a rare neural tube defect characterized by extreme retroflexion of the head with the absence of neck due to spinal deformities. The important features that help us to diagnose a case of iniencephaly are occipital bone deficit leading to enlarged foramen magnum, fusion of malformed ce...

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Autores principales: Kulkarni, Padmaja R., Rao, Ravikala V., Alur, Mohan B., Joshi, S. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296405/
https://www.ncbi.nlm.nih.gov/pubmed/22408660
http://dx.doi.org/10.4103/1817-1745.92831
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author Kulkarni, Padmaja R.
Rao, Ravikala V.
Alur, Mohan B.
Joshi, S. K.
author_facet Kulkarni, Padmaja R.
Rao, Ravikala V.
Alur, Mohan B.
Joshi, S. K.
author_sort Kulkarni, Padmaja R.
collection PubMed
description Iniencephaly is a rare neural tube defect characterized by extreme retroflexion of the head with the absence of neck due to spinal deformities. The important features that help us to diagnose a case of iniencephaly are occipital bone deficit leading to enlarged foramen magnum, fusion of malformed cervical and thoracic vertebrae, and upward turned face with chin continuous with chest because of the absence of neck. The differential diagnoses include anencephaly with spinal retroflexion, Klippel–Fiel syndrome, nuchal tumors such as teratoma, goiter, and lymphangioma and Jarcho–Levin syndrome. Previously many case reports on radiological features of iniencephaly are published, but there are very few articles on necropsy findings and differential diagnosis. In the present case we have discussed in detail the necropsy findings of iniencephaly clausus with special reference to differential diagnosis.
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spelling pubmed-32964052012-03-09 Iniencephaly clausus: A case report with review of literature Kulkarni, Padmaja R. Rao, Ravikala V. Alur, Mohan B. Joshi, S. K. J Pediatr Neurosci Case Report Iniencephaly is a rare neural tube defect characterized by extreme retroflexion of the head with the absence of neck due to spinal deformities. The important features that help us to diagnose a case of iniencephaly are occipital bone deficit leading to enlarged foramen magnum, fusion of malformed cervical and thoracic vertebrae, and upward turned face with chin continuous with chest because of the absence of neck. The differential diagnoses include anencephaly with spinal retroflexion, Klippel–Fiel syndrome, nuchal tumors such as teratoma, goiter, and lymphangioma and Jarcho–Levin syndrome. Previously many case reports on radiological features of iniencephaly are published, but there are very few articles on necropsy findings and differential diagnosis. In the present case we have discussed in detail the necropsy findings of iniencephaly clausus with special reference to differential diagnosis. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3296405/ /pubmed/22408660 http://dx.doi.org/10.4103/1817-1745.92831 Text en Copyright: © Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kulkarni, Padmaja R.
Rao, Ravikala V.
Alur, Mohan B.
Joshi, S. K.
Iniencephaly clausus: A case report with review of literature
title Iniencephaly clausus: A case report with review of literature
title_full Iniencephaly clausus: A case report with review of literature
title_fullStr Iniencephaly clausus: A case report with review of literature
title_full_unstemmed Iniencephaly clausus: A case report with review of literature
title_short Iniencephaly clausus: A case report with review of literature
title_sort iniencephaly clausus: a case report with review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296405/
https://www.ncbi.nlm.nih.gov/pubmed/22408660
http://dx.doi.org/10.4103/1817-1745.92831
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