Abstract
The authors performed genetic analyses and Sanger sequencing, identifying a homozygous deletion of GRID2 exon 4 in the index family and compound heterozygous deletions involving GRID2 exon 2 in a second family. Biallelic deletions of GRID2 may lead to a syndrome of cerebellar ataxia and tonic upgaze in affected individuals. See p. 1378 Of 926 patients diagnosed with migraine, 375 had MRIs and 115 had abnormalities, with 39 having white matter lesions. The prevalence of white matter lesions is more common in pediatric migraine with aura, but they appear to be …
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