Epilepsy and outcome in FOXG1-related disorders

OBJECTIVE: FOXG1-related disorders are associated with severe intellectual disability, absent speech with autistic features, and epilepsy. Children with deletions or intragenic mutations of FOXG1 also have postnatal microcephaly, morphologic abnormalities of the corpus callosum, and choreiform movem...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Epilepsia
Main Authors: Seltzer, Laurie E., Ma, Mandy, Ahmed, Sohnee, Bertrand, Mary, Dobyns, William B., Wheless, James, Paciorkowski, Alex R.
Format: Artigo
Jezik:Inglês
Izdano: 2014
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4265461/
https://ncbi.nlm.nih.gov/pubmed/24836831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.12648
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