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

Medicina (Kaunas). 2020 Aug 1;56(8):387. doi: 10.3390/medicina56080387.

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.

Keywords: DHRS9; GABA; NGS; allopregnanolone; exome; temporal lobe epilepsy.

Publication types

  • Case Reports

MeSH terms

  • 3-Hydroxysteroid Dehydrogenases / analysis*
  • 3-Hydroxysteroid Dehydrogenases / blood
  • Causality*
  • Child, Preschool
  • Epilepsy / diagnosis
  • Epilepsy / epidemiology
  • Epilepsy / genetics*
  • Female
  • Humans
  • Mutation, Missense / genetics
  • Polymorphism, Genetic / genetics
  • Temporal Lobe / abnormalities
  • Temporal Lobe / diagnostic imaging

Substances

  • 3-Hydroxysteroid Dehydrogenases
  • DHRS9 protein, human