Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Erratum to: Epilepsy and Other Neuropsychiatric Manifestations in Children and Adolescents with 22q11.2 Deletion Syndrome
por: Kim, Eun-Hee, et al.
Publicado: (2016) -
Psychotic Features as the First Manifestation of 22q11.2 Deletion Syndrome
por: Kook, So Dahm, et al.
Publicado: (2010) -
Various Psychiatric Manifestation in DiGeorge Syndrome (22q11.2 Deletion Syndrome): A Case Report
por: Kim, Giok, et al.
Publicado: (2020) -
Epilepsy, neuropsychiatric phenotypes, neuroimaging findings, and genotype-neurophenotype correlation in 22q11.2 deletion syndrome
por: AlKalaf, Heeba Y., et al.
Publicado: (2020) -
Delayed Diagnosis of Chromosome 22q11.2 Deletion Syndrome Due to Late-Onset Generalized Epilepsy
por: Lee, Seon-Kyung, et al.
Publicado: (2020)