Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation

The neurodevelopmental progression of a school‐aged child with a spontaneous IQSEC2 mutation has demonstrated apparent regression of milestones and language. Seizures associated with the disorder have been refractory to medical treatment. Late treatment of autism in this child has led to improved so...

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Udgivet i:Clin Case Rep
Main Authors: Zipper, Rachelle, Baine, Sherri D., Genizi, Jacob, Maoz, Hen, Levy, Nina S., Levy, Andrew P.
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2017
Fag:
Case Reports
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5628232/
https://ncbi.nlm.nih.gov/pubmed/29026562
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1139
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