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Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report

Authors :
Francesco Calì
Maurizio Elia
Mirella Vinci
Luigi Vetri
Edvige Correnti
Emanuele Trapolino
Michele Roccella
Francesca Vanadia
Valentino Romano
Source :
Medicina, Vol 56, Iss 8, p 387 (2020)
Publication Year :
2020
Publisher :
MDPI AG, 2020.

Abstract

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.

Details

Language :
English
ISSN :
56080387, 16489144, and 1010660X
Volume :
56
Issue :
8
Database :
Directory of Open Access Journals
Journal :
Medicina
Publication Type :
Academic Journal
Accession number :
edsdoj.96d79a889164b729491857dcf90fab9
Document Type :
article
Full Text :
https://doi.org/10.3390/medicina56080387