Genetic and neurobiological aspects of comorbid occurence of autism spectrum disorder and epilepsy
Authors:
P. Danhofer 1; O. Horák 1; Š. Aulická 1; K. Česká 1; J. Pejčochová 1; L. Fajkusová 2; H. Ošlejšková 1
Authors place of work:
Klinika dětské neurologie LF MU a FN Brno, Centrum pro epilepsie Brno
1; Centrum molekulární biologie a genové terapie Interní hematoonkologické kliniky LF MU a FN Brno
2
Published in the journal:
Cesk Slov Neurol N 2019; 82(2): 148-154
Category:
Review Article
doi:
https://doi.org/10.14735/amcsnn2019148
Summary
Autism spectrum disorder (ASD) is ranked among neurodevelopmental and neuropsychiatric disorders with clinical onset in childhood. In recent years, this disorder has come to the forefront of scientific interest, mainly due to increasing prevalence of up to 1/ 68 in 2014. The genetic causes of the disorder and the pathophysiological mechanisms that might be involved in the development of ASD are revealed. Comorbid occurrence with epilepsy is quite common, in up to 46% of cases. This article summarizes the current knowledge in this field with a focus on the hypothesis of excitatory-inhibitory imbalance. Some genetic causes of ASD and current diagnostic options are also discussed. The pathophysiology of the co-morbidity of ASD and epilepsy is discussed in terms of possible therapeutic interventions.
Keywords:
Genetics – Autism – Epilepsy – Autism spectrum disorder – ASD
Zdroje
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Štítky
Paediatric neurology Neurosurgery NeurologyČlánok vyšiel v časopise
Czech and Slovak Neurology and Neurosurgery
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