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

Central nervous system vascular malformation Chromosome 17 duplication Genetic disorder

Journal

Journal of cerebrovascular and endovascular neurosurgery
ISSN: 2234-8565
Titre abrégé: J Cerebrovasc Endovasc Neurosurg
Pays: Korea (South)
ID NLM: 101589154

Informations de publication

Date de publication:
26 Dec 2023
Historique:
received: 11 07 2023
accepted: 24 11 2023
medline: 26 12 2023
pubmed: 26 12 2023
entrez: 25 12 2023
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 38146067
pii: jcen.2023.E2023.07.001
doi: 10.7461/jcen.2023.E2023.07.001
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Shiwei Huang (S)

Department of Neurosurgery, University of Minnesota, MN, USA.

William Dobyns (W)

Department of Pediatrics, Division of Pediatric Genetics & Metabolism, University of Minnesota, MN, USA.

Corinne Duncan (C)

Department of Radiology, University of Minnesota, MN, USA.

David Nascene (D)

Department of Radiology, University of Minnesota, MN, USA.

Classifications MeSH