Genetic Basis of Hypsarrhythmia: Expanding the PHACTR1 Spectrum and Pathway to Targeted Therapy

Karen Willième1, Annelies Dheedene2, Arnaud Vanlander1

  • 1Department of Paediatrics, Division Paediatric Neurology, Ghent University Hospital, Ghent, Belgium.

Clinical Genetics
|October 7, 2025
PubMed

Insights

A novel PHACTR1 gene variant was identified in an infant with infantile spasms and hypsarrhythmia. This finding highlights a potential therapeutic target involving the PHACTR1 and Slack channel pathway for epilepsy treatment.

Area of Science:

  • Genetics
  • Neurology
  • Molecular Biology

Background:

  • Infantile spasms and hypsarrhythmia are severe epilepsy syndromes in infants.
  • The PHACTR1 gene encodes a protein involved in cytoskeletal regulation and signaling.
  • Slack (KCNT1) channels are sodium-activated potassium channels implicated in various epilepsy types.

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