ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview

Greta Amore1, Elisa Calì2, Maria Spanò3

  • 1Department of Neuromuscular Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, United Kingdom; Unit of Child Neurology and Psychiatry, Department of Human Pathology of the Adult and Developmental Age "Gaetano Barresi", University of Messina, Via C. Valeria 1, 98125 Messina, Italy.

Brain & Development
|August 26, 2023
PubMed
Summary

A novel ATP6V1B2 gene variant was identified in a patient with global developmental delay and epileptic encephalopathy. This finding expands the known spectrum of ATP6V1B2-related disorders, including developmental epileptic encephalopathies.

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