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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...

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Autores principales: Chekhlabi, Nabila, Haoudar, Amal, Hamdaoui, Hasna, Dini, Nezha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
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.
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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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