| Literature DB >> 24630051 |
Ginevra Zanni1, Sabina Barresi2, Roni Cohen3, Nicola Specchio4, Lina Basel-Vanagaite3, Enza Maria Valente5, Avinoam Shuper3, Federico Vigevano4, Enrico Bertini2.
Abstract
Mutations in the solute carrier family 9, subfamily A member 6 (SLC9A6) gene, encoding the endosomal Na+/H+ exchanger 6 (NHE6) are associated with Christianson syndrome, a syndromic form of X-linked intellectual disability characterized by microcephaly, severe global developmental delay, autistic behavior, early onset seizures and ataxia. In a 7-year-old boy with characteristic clinical and neuroimaging features of Christianson syndrome and epileptic encephalopathy with continuous spikes and waves during sleep, we identified a novel splice site mutation (IVS10-1G>A) in SLC9A6. These findings expand the clinical spectrum of the syndrome and indicate NHE6 dysfunction as a new cause of electrical status epilepticus during slow-wave sleep (ESES).Entities:
Keywords: Christianson syndrome; ESES; NHE6; SLC9A6
Mesh:
Substances:
Year: 2014 PMID: 24630051 DOI: 10.1016/j.eplepsyres.2014.02.009
Source DB: PubMed Journal: Epilepsy Res ISSN: 0920-1211 Impact factor: 3.045