Diffuse CNS cortical vein malformations with chromosome 17q microduplication: Possible link to SEC14L1

Shiwei Huang, William Dobyns, Corinne Duncan, David Nascene

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
Pages (from-to)298-303
Number of pages6
JournalJournal of Cerebrovascular and Endovascular Neurosurgery
Volume26
Issue number3
DOIs
StatePublished - 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

Fingerprint

Dive into the research topics of 'Diffuse CNS cortical vein malformations with chromosome 17q microduplication: Possible link to SEC14L1'. Together they form a unique fingerprint.

Cite this