Neuropediatrics · 2015 · 20 citations · 9 references
Life SciencesGeneticsNeurologyHuman GeneticsMedical GeneticsNeuroradiologyCongenital Brain MalformationsCongenital DisordersGenetic DisordersGenetic EpilepsiesMendelian DisordersNeurogenetic DisordersCongenital Neurologic MalformationsGenetic Causes Of EpilepsyGenetic Epilepsies In ChildrenGenetic Epilepsy SyndromesMalformation EtiologyMendelian Neurodevelopmental DisordersPediatric Neurogenetic DisordersSyndromic Epilepsy
Loss of function of GPR56 causes a specific brain malformation called the bilateral frontoparietal polymicrogyria (BFPP), which has typical clinical and neuroradiological findings. So far, 35 families and 26 independent mutations have been described.We present a Portuguese 5-year-old boy, born from nonconsanguineous parents, with BFPP. This patient has a novel GPR56 mutation (R271X) and an unusual phenotype, because he presents hot water epilepsy.To the best of our knowledge, this is the first reported case of BFPP evolving hot water epilepsy.
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G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex
Xianhua Piao, R. Sean Hill, Adria Bodell et al. · Science · 2004 · 522 citations
Genotype–phenotype analysis of human frontoparietal polymicrogyria syndromes
Xianhua Piao, Bernard S. Chang, Adria Bodell et al. · Annals of Neurology · 2005 · 153 citations · Full text