Synapsins are neuron-specific phosphoproteins that modulate neurotransmitter release, synaptic plasticity, and molecular processes shaping higher brain functions. Pathogenic synapsin-1 () variants are associated with epilepsy, intellectual disabilities, and behavioral problems. We detected a novel variant [c.477_479delTGG (p.Gly160del)] in brothers with focal epilepsy with secondary generalization. The deleted amino acid was found to be highly conserved among mammalian species. In electroencephalography, the older brother showed a bioelectrical status epilepticus and was also diagnosed with attention deficit hyperactivity disorder. Behavioral abnormalities were seen before or after the seizures. Both patients responded quickly to treatment with valproate. Our case reports are consistent with the clinical heterogeneity of the pathogenic variants described in the literature.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1055/a-2019-0136 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!