PREVALENCE AND AETIOLOGY OF EPILEPTIC SEIZURES IN YOUNG PEOPLE WITH 22Q11.2 DELETION SYNDROME AND RELATIONSHIPS WITH OTHER NEURODEVELOPMENTAL DISORDERS

被引：0

作者：

Eaton, C. B. ^{[1
,2
]}

Thomas, R. H. ^{[1
,3
]}

Hamandi, K. H. ^{[4
]}

Payne, G. C. ^{[5
]}

Kerr, M. P. ^{[1
]}

Linden, D. E. J. ^{[1
,6
]}

Owen, M. J. ^{[1
]}

Cunningham, A. C. ^{[1
]}

Bartsch, U. B. ^{[7
,8
]}

Struik, S. S. ^{[9
]}

van denBree, M. B. M. ^{[1
]}

机构：

[1] Cardiff Univ, Sch Med, Div Psychol Med & Clin Neurosci, MRC Ctr Neuropsychiat Genet & Genom, Cardiff, S Glam, Wales

[2] Univ Birmingham, Sch Psychol, Cerebra Ctr Neurodev Disorders, Birmingham, W Midlands, England

[3] Newcastle Univ, Inst Neurosci, Newcastle Upon Tyne, Tyne & Wear, England

[4] Univ Hosp Wales, Epilepsy Unit, Heath Pk, Cardiff, S Glam, Wales

[5] Betsi Cadwaladr Univ Healthboard, Bangor, Gwynedd, Wales

[6] Maastricht Univ, Fac Hlth Med & Life Sci, Sch Mental Hlth & Neurosci, Maastricht, Netherlands

[7] Univ Bristol, Sch Physiol Pharmacol & Neurosci, Bristol, Avon, England

[8] Lilly UK, Erl Wood Manor, Windlesham, Surrey, England

[9] Univ Hosp Wales, Immunodeficiency Ctr Wales, Cardiff, S Glam, Wales

来源：

关键词：

22q11.2 deletion syndrome; cognition; epilepsy; genetics; neurodevelopmental disorder; seizure;

D O I：

暂无

中图分类号：

G76 [特殊教育];

学科分类号：

040109 ;

摘要：

引用

页码：1080 / 1080

页数：1