Biallelic SZT2 mutation with early onset of focal status epilepticus: useful diagnostic clues other than epilepsy, intellectual disability and macrocephaly

We read with great interest the paper entitled “Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly” by Domingues et al. [1].

Source: Seizure: European Journal of Epilepsy - May 18, 2019 Category: Neurology Authors: Alessandro Iodice, Carlotta Spagnoli, Daniele Frattini, Grazia Gabriella Salerno, Susanna Rizzi, Carlo Fusco Tags: Letter to the editor Source Type: research