Fig. 6
From: Expanding genotype–phenotype correlations in FOXG1 syndrome: results from a patient registry
Epilepsy characteristics reported in FOXG1 syndrome. For those individuals with a reported history of epilepsy, caregivers were asked to describe the epilepsy phenotype in their child or ward as part of the FOXG1 syndrome patient registry. Proportions of age range for seizure onset are depicted (A) in addition to distributions of seizure frequency at worst (B) and optimal (C) seizure control. Comparisons between genotypes were evaluated using Kruskal–Wallis test with Dunn’s test to correct for multiple comparisons, #p < 0.05