0000000000898533

AUTHOR

Joseph B. Hiatt

showing 1 related works from this author

PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia

2015

Malformations of cortical development containing dysplastic neuronal and glial elements, including hemimegalencephaly and focal cortical dysplasia, are common causes of intractable paediatric epilepsy. In this study we performed multiplex targeted sequencing of 10 genes in the PI3K/AKT pathway on brain tissue from 33 children who underwent surgical resection of dysplastic cortex for the treatment of intractable epilepsy. Sequencing results were correlated with clinical, imaging, pathological and immunohistological phenotypes. We identified mosaic activating mutations in PIK3CA and AKT3 in this cohort, including cancer-associated hotspot PIK3CA mutations in dysplastic megalencephaly, hemimeg…

MaleHemimegalencephalyPathologymedicine.medical_specialtyAKT3HemimegalencephalyPhosphatidylinositol 3-KinasesmedicinePTENHumansMegalencephalyPI3K/AKT/mTOR pathwaybiologyBrainOriginal ArticlesCortical dysplasiamedicine.diseaseDEPDC5MegalencephalyMalformations of Cortical DevelopmentDysplasiabiology.proteinFemaleNeurology (clinical)Proto-Oncogene Proteins c-aktSignal Transduction
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