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

Author:

Calì FrancescoORCID,Elia Maurizio,Vinci MirellaORCID,Vetri LuigiORCID,Correnti EdvigeORCID,Trapolino Emanuele,Roccella MicheleORCID,Vanadia Francesca,Romano Valentino

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.

Funder

The Italian Ministry of Health

Publisher

MDPI AG

Subject

General Medicine

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