| Literature DB >> 25642806 |
Rita Santos-Silva1, Armanda Passas1, Carla Rocha1, Rita Figueiredo2, Jose Mendes-Ribeiro3, Susana Fernandes4, Saskia Biskup5, Miguel Leão6.
Abstract
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. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2015 PMID: 25642806 DOI: 10.1055/s-0034-1399754
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947