| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8690585 | Pediatric Neurology | 2017 | 18 Pages |
Abstract
Patients with structural brain abnormalities, especially polymicrogyria and associated epilepsy should have a chromosomal microarray (CMA) performed to screen for the 22q11.2 deletion syndrome. Focal epilepsy and genetic generalized epilepsy are the most frequent epilepsy types reported in this condition.
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Authors
Basanagoud MD, Sunitha MD, Stephen MD, Ehab MD, James W. MD,