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Our patient had a chromosomal 16p13.11 microdeletion that confers susceptibility to various types of epilepsy. This is the first report detailing an association of hemiconvulsion-hemiplegia-epilepsy syndrome with a 16p13.11 deletion and identifies another potential causal factor for hemiconvulsion-hemiplegia-epilepsy syndrome.<\/jats:p>","DOI":"10.1177\/0883073813516382","type":"journal-article","created":{"date-parts":[[2014,1,22]],"date-time":"2014-01-22T20:14:35Z","timestamp":1390421675000},"page":"83-86","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":6,"title":["16p13.11 Microdeletion in a Patient With Hemiconvulsion-Hemiplegia-Epilepsy Syndrome"],"prefix":"10.1177","volume":"30","author":[{"given":"Christina I.","family":"Miteff","sequence":"first","affiliation":[{"name":"John Hunter Children's Hospital, New Lambton Heights, New South Wales, Australia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert L.","family":"Smith","sequence":"additional","affiliation":[{"name":"John Hunter Children's 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