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Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report
The DHRS9 gene is involved in several pathways including the synthesis of allopregnanolone from progesterone. Allopregnanolone is a positive modulator of gamma aminobutyric acid (GABA) action and plays a role in the control of neuronal excitability and seizures. Whole-exome sequencing performed on a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466289/ https://www.ncbi.nlm.nih.gov/pubmed/32752300 http://dx.doi.org/10.3390/medicina56080387 |
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author | Calì, Francesco Elia, Maurizio Vinci, Mirella Vetri, Luigi Correnti, Edvige Trapolino, Emanuele Roccella, Michele Vanadia, Francesca Romano, Valentino |
author_facet | Calì, Francesco Elia, Maurizio Vinci, Mirella Vetri, Luigi Correnti, Edvige Trapolino, Emanuele Roccella, Michele Vanadia, Francesca Romano, Valentino |
author_sort | Calì, Francesco |
collection | PubMed |
description | The DHRS9 gene is involved in several pathways including the synthesis of allopregnanolone from progesterone. Allopregnanolone is a positive modulator of gamma aminobutyric acid (GABA) action and plays a role in the control of neuronal excitability and seizures. Whole-exome sequencing performed on a girl with an early onset epilepsy revealed that she was a compound heterozygote for two novel missense mutations of the DHRS9 gene likely to disrupt protein function. No previous studies have reported the implication of this gene in epilepsy. We discuss a new potential pathogenic mechanism underlying epilepsy in a child, due to a defective progesterone pathway. |
format | Online Article Text |
id | pubmed-7466289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74662892020-09-14 Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report Calì, Francesco Elia, Maurizio Vinci, Mirella Vetri, Luigi Correnti, Edvige Trapolino, Emanuele Roccella, Michele Vanadia, Francesca Romano, Valentino Medicina (Kaunas) Case Report The DHRS9 gene is involved in several pathways including the synthesis of allopregnanolone from progesterone. Allopregnanolone is a positive modulator of gamma aminobutyric acid (GABA) action and plays a role in the control of neuronal excitability and seizures. Whole-exome sequencing performed on a girl with an early onset epilepsy revealed that she was a compound heterozygote for two novel missense mutations of the DHRS9 gene likely to disrupt protein function. No previous studies have reported the implication of this gene in epilepsy. We discuss a new potential pathogenic mechanism underlying epilepsy in a child, due to a defective progesterone pathway. MDPI 2020-08-01 /pmc/articles/PMC7466289/ /pubmed/32752300 http://dx.doi.org/10.3390/medicina56080387 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Report Calì, Francesco Elia, Maurizio Vinci, Mirella Vetri, Luigi Correnti, Edvige Trapolino, Emanuele Roccella, Michele Vanadia, Francesca Romano, Valentino Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title | Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title_full | Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title_fullStr | Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title_full_unstemmed | Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title_short | Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report |
title_sort | are mutations in the dhrs9 gene causally linked to epilepsy? a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466289/ https://www.ncbi.nlm.nih.gov/pubmed/32752300 http://dx.doi.org/10.3390/medicina56080387 |
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