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• W2922229802 abstract "Background Children with tuberous sclerosis complex (TSC), caused by pathogenic variants in TSC1/TSC2, are at risk for intellectual disability. TSC2 pathogenic variants appear to increase the risk, compared with TSC1. However, the effect of TSC2 pathogenic variants on early and specific domains of development hasn’t been studied. Using an extensively phenotyped group, we aimed to characterize differences in early intellectual development between genotypes. Methods The study group (n = 92) included participants with TSC enrolled in a multicenter study involving genetic testing and detailed prospective phenotyping including the Mullen Scales of Early Learning, a validated measure of cognition, language, and motor development in babies and preschool children. Mean T-scores at 24 months for each Mullen Scales of Early Learning domain were calculated for children with, versus without, a TSC2 pathogenic variant. Multivariable linear regression models were used to compare the groups, adjusting for seizures. Results T-scores on every Mullen Scales of Early Learning domain were significantly worse in the TSC2 group. Below average composite scores were present in three-fourths of the TSC2 group, compared with one-fourth of those without TSC2. Having a TSC2 pathogenic variant was associated with lower composite Mullen Scales of Early Learning scores, even when corrected for seizures. Conclusions In a well-characterized patient population with standardized assessment of multiple aspects of development, we found that having a TSC2 pathogenic variant was associated with significantly lower Mullen Scales of Early Learning scores at age 24 months, independent of seizures. These data suggest that a baby with a TSC2 pathogenic variant is at high risk for significant developmental delays by 24 months." @default.
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• W2922229802 date "2019-07-01" @default.
• W2922229802 modified "2023-10-06" @default.
• W2922229802 title "Tuberous Sclerosis Complex Genotypes and Developmental Phenotype" @default.
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• W2922229802 doi "https://doi.org/10.1016/j.pediatrneurol.2019.03.003" @default.
• W2922229802 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6837240" @default.
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