Dravet syndrome is rare genetic epilepsy syndrome and epileptic encephalopathy. The patient initially has normal developmental profile with plateau or regression that begins after seizure onset. We report a case of two-year-old child diagnosed as dravet syndrome with moderate cerebral atrophy and ventricular dilatation as rare MRI finding.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069364 | PMC |
| http://dx.doi.org/10.1002/ccr3.5840 | DOI Listing |
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