Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5626825 | Brain and Development | 2017 | 5 Pages |
Abstract
We report three additional cases of this rare condition, expanding the clinical and pathological phenotype. We performed trio whole exome sequencing, the first in this cohort of patients, and did not identify a pathogenic variant. As postulated in the original report, the likely underlying mechanism is antenatal hypoxia in the third trimester.
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Authors
Gorman Kathleen Mary, Aird John James, Conroy Judith, Devaney Deirdre, Farrell Michael, King Mary Dolores,