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A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant
Arnold Chiari malformation is one of the commonest cause of congenital hydrocephalus. Cause of fetal development of cerebellar tonsils remains unknown and may be diagnosed at later in life. The association of Arnold Chiari malformation with acromesomelic dwarfism is not known. We report male infant...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017357/ https://www.ncbi.nlm.nih.gov/pubmed/33854687 http://dx.doi.org/10.11604/pamj.2021.38.58.27295 |
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author | Maurya, Miteshkumar Rajaram Ravi, Renju Pungavkar, Sona Ajit |
author_facet | Maurya, Miteshkumar Rajaram Ravi, Renju Pungavkar, Sona Ajit |
author_sort | Maurya, Miteshkumar Rajaram |
collection | PubMed |
description | Arnold Chiari malformation is one of the commonest cause of congenital hydrocephalus. Cause of fetal development of cerebellar tonsils remains unknown and may be diagnosed at later in life. The association of Arnold Chiari malformation with acromesomelic dwarfism is not known. We report male infant diagnosed with acromesomelic dwarfism at end of gestation period on basis of antenatal ultrasonography findings. An ultrasound scan of infant head at fifth month of birth was performed in view of increasing head circumference that revealed aqueductal stenosis with dilated posterior horn of lateral ventricles in brain. |
format | Online Article Text |
id | pubmed-8017357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-80173572021-04-13 A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant Maurya, Miteshkumar Rajaram Ravi, Renju Pungavkar, Sona Ajit Pan Afr Med J Case Report Arnold Chiari malformation is one of the commonest cause of congenital hydrocephalus. Cause of fetal development of cerebellar tonsils remains unknown and may be diagnosed at later in life. The association of Arnold Chiari malformation with acromesomelic dwarfism is not known. We report male infant diagnosed with acromesomelic dwarfism at end of gestation period on basis of antenatal ultrasonography findings. An ultrasound scan of infant head at fifth month of birth was performed in view of increasing head circumference that revealed aqueductal stenosis with dilated posterior horn of lateral ventricles in brain. The African Field Epidemiology Network 2021-01-18 /pmc/articles/PMC8017357/ /pubmed/33854687 http://dx.doi.org/10.11604/pamj.2021.38.58.27295 Text en Copyright: Miteshkumar Rajaram Maurya et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Maurya, Miteshkumar Rajaram Ravi, Renju Pungavkar, Sona Ajit A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title | A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title_full | A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title_fullStr | A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title_full_unstemmed | A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title_short | A case report of Arnold Chiari type 1 malformation in acromesomelic dwarf infant |
title_sort | case report of arnold chiari type 1 malformation in acromesomelic dwarf infant |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017357/ https://www.ncbi.nlm.nih.gov/pubmed/33854687 http://dx.doi.org/10.11604/pamj.2021.38.58.27295 |
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