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

Francesco CalìMaurizio EliaMirella VinciLuigi VetriEdvige CorrentiEmanuele TrapolinoMichele RoccellaFrancesca VanadiaValentino Romano
Published in: Medicina (Kaunas, Lithuania) (2020)
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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