Cargando…
Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders
OBJECTIVE: The true prevalence of epileptic seizures and epilepsy in 22q11.2 deletion syndrome (22q11.2DS) is unknown, because previous studies have relied on historical medical record review. Associations of epilepsy with other neurodevelopmental manifestations (eg, specific psychiatric diagnoses)...
Autores principales: | Eaton, Christopher B., Thomas, Rhys H., Hamandi, Khalid, Payne, Gareth C., Kerr, Michael P., Linden, David E. J., Owen, Michael J., Cunningham, Adam C., Bartsch, Ullrich, Struik, Siske S., van den Bree, Marianne B. M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519005/ https://www.ncbi.nlm.nih.gov/pubmed/30977115 http://dx.doi.org/10.1111/epi.14722 |
Ejemplares similares
-
Sleep EEG in young people with 22q11.2 deletion syndrome: A cross-sectional study of slow-waves, spindles and correlations with memory and neurodevelopmental symptoms
por: Donnelly, Nicholas A, et al.
Publicado: (2022) -
Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome
por: Cunningham, Adam C., et al.
Publicado: (2018) -
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
por: Cunningham, Adam C., et al.
Publicado: (2019) -
Clinical Characteristics of Seizures and Epilepsy in Individuals With Recurrent Deletions and Duplications in the 16p11.2 Region
por: Moufawad El Achkar, Christelle, et al.
Publicado: (2022) -
Psychiatric disorders in children with 16p11.2 deletion and duplication
por: Niarchou, Maria, et al.
Publicado: (2019)