Are mutations in the dhrs9 gene causally linked to epilepsy? A case report

Valentino Romano, Michele Roccella, Mirella Vinci, Francesco Calì, Luigi Vetri, Emanuele Trapolino, Francesca Vanadia, Maurizio Elia, Edvige Correnti, Luigi Vetri

Research output: Contribution to journalArticlepeer-review

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.
Original languageEnglish
Pages (from-to)1-4
Number of pages4
JournalMedicina
Volume56
Publication statusPublished - 2020

All Science Journal Classification (ASJC) codes

  • General Medicine

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