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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...

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Autores principales: Calì, Francesco, Elia, Maurizio, Vinci, Mirella, Vetri, Luigi, Correnti, Edvige, Trapolino, Emanuele, Roccella, Michele, Vanadia, Francesca, Romano, Valentino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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