Abstract
Partial trisomy of the long arm of chromosome 17 (17q) is a rare but clinically recognized syndrome that involves facial dysmorphisms, skeletal abnormalities, and global developmental delay, as well as various reports of cardiovascular, renal, and central nervous system abnormalities. This report presents a novel neuroradiologic finding of diffuse enlarged, tortuous cortical veins with physiological antegrade flow in a child with a microduplication of the distal end of 17q. To our knowledge, this finding has not been described previously. Although the exact cause for the cortical vascular anomaly is currently unknown, this duplicated region contains genes of interest for future studies that focus on normal and abnormal angiogenesis.
Original language | English (US) |
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Pages (from-to) | 298-303 |
Number of pages | 6 |
Journal | Journal of Cerebrovascular and Endovascular Neurosurgery |
Volume | 26 |
Issue number | 3 |
DOIs | |
State | Published - Sep 1 2024 |
Bibliographical note
Publisher Copyright:© 2024 by KSCVS and KoNES.
Keywords
- Central nervous system vascular malformation
- Genetic disorder
- Chromosome 17 duplication
PubMed: MeSH publication types
- Case Reports
- Journal Article