Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome

BACKGROUND AND PURPOSE: 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion syndrome. Epilepsy and other neuropsychiatric (NP) manifestations of this genetic syndrome are not uncommon, but they are also not well-understood. We sought to identify the characteristics of epilepsy and...

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Detalles Bibliográficos
Autores principales: Kim, Eun-Hee, Yum, Mi-Sun, Lee, Beom-Hee, Kim, Hyo-Won, Lee, Hyun-Jeoung, Kim, Gu-Hwan, Lee, Yun-Jeong, Yoo, Han-Wook, Ko, Tae-Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712291/
https://www.ncbi.nlm.nih.gov/pubmed/26754781
http://dx.doi.org/10.3988/jcn.2016.12.1.85

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712291/
https://www.ncbi.nlm.nih.gov/pubmed/26754781
http://dx.doi.org/10.3988/jcn.2016.12.1.85

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