JOURNAL ARTICLE

Fragile Females: Case Series of Epilepsy in Girls With FMR1 Disruption

Kenneth A Myers, Femke N G van 't Hof, Lynette G Sadleir, Geneviève Legault, Elisabeth Simard-Tremblay, David J Amor, Ingrid E Scheffer
Pediatrics 2019, 144 (3)
31439621
Girls with pathogenic variants in FMR1 , the gene responsible for Fragile X syndrome, have received relatively little attention in the literature. The reports of girls with trinucleotide expansions or deletions affecting FMR1 describe variable phenotypes; having normal intelligence and no severe neurologic sequelae is not uncommon. We reviewed epilepsy genetics research databases for girls with FMR1 pathogenic variants and seizures to characterize the spectrum of epilepsy phenotypes. We identified 4 patients, 3 of whom had drug-resistant focal epilepsy. Two had severe developmental and epileptic encephalopathy with late-onset epileptic spasms. Our findings demonstrate that FMR1 loss-of-function variants can result in severe neurologic phenotypes in girls. Similar cases may be missed because clinicians may not always perform Fragile X testing in girls, particularly those with severe neurodevelopmental impairment or late-onset spasms.

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