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Report of a New Case of Pentasomy X Revealed by Status Epilepticus
This report describes an exceptional case of X (49, XXXXX) pentasomy in a girl aged three years and five months. She was admitted for recurrent seizures revealing epilepsy. She has growth failure and psychomotor retardation with a deformed face. The malformative assessment did not show any malformat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330396/ https://www.ncbi.nlm.nih.gov/pubmed/34367739 http://dx.doi.org/10.7759/cureus.16062 |
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author | Chekhlabi, Nabila Haoudar, Amal Hamdaoui, Hasna Dini, Nezha |
author_facet | Chekhlabi, Nabila Haoudar, Amal Hamdaoui, Hasna Dini, Nezha |
author_sort | Chekhlabi, Nabila |
collection | PubMed |
description | This report describes an exceptional case of X (49, XXXXX) pentasomy in a girl aged three years and five months. She was admitted for recurrent seizures revealing epilepsy. She has growth failure and psychomotor retardation with a deformed face. The malformative assessment did not show any malformation apart from cerebral leukodystrophy. Pentasomy X is a very rare abnormality of the sex chromosomes. It only affects females, in whom three additional X chromosomes are added to the two X normally present. The pathogenesis of pentasomy X is not exactly clear, but it is probably caused by successive maternal nondisjunctions. Epilepsy and cerebral leukodystrophy are a new mode of revelation of this syndrome, never described in the literature. |
format | Online Article Text |
id | pubmed-8330396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-83303962021-08-06 Report of a New Case of Pentasomy X Revealed by Status Epilepticus Chekhlabi, Nabila Haoudar, Amal Hamdaoui, Hasna Dini, Nezha Cureus Genetics This report describes an exceptional case of X (49, XXXXX) pentasomy in a girl aged three years and five months. She was admitted for recurrent seizures revealing epilepsy. She has growth failure and psychomotor retardation with a deformed face. The malformative assessment did not show any malformation apart from cerebral leukodystrophy. Pentasomy X is a very rare abnormality of the sex chromosomes. It only affects females, in whom three additional X chromosomes are added to the two X normally present. The pathogenesis of pentasomy X is not exactly clear, but it is probably caused by successive maternal nondisjunctions. Epilepsy and cerebral leukodystrophy are a new mode of revelation of this syndrome, never described in the literature. Cureus 2021-06-30 /pmc/articles/PMC8330396/ /pubmed/34367739 http://dx.doi.org/10.7759/cureus.16062 Text en Copyright © 2021, Chekhlabi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Genetics Chekhlabi, Nabila Haoudar, Amal Hamdaoui, Hasna Dini, Nezha Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title | Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title_full | Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title_fullStr | Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title_full_unstemmed | Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title_short | Report of a New Case of Pentasomy X Revealed by Status Epilepticus |
title_sort | report of a new case of pentasomy x revealed by status epilepticus |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8330396/ https://www.ncbi.nlm.nih.gov/pubmed/34367739 http://dx.doi.org/10.7759/cureus.16062 |
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