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Article

Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation.

Clinical genetics - 1 Sept 2014

Sheikhzadeh S, Sondermann C, Rybczynski M, Habermann C R, Brockstaedt L, Keyser B, Kaemmerer H, Mir T, Staebler A, Robinson P N, Kutsche K, Berger J, Blankenberg S, von Kodolitsch Y

Abstract excerpt

The purpose of this study was to perform a comprehensive study of dural ectasia (DE) related to FBN1 mutations. We performed a database analysis of two German metropolitan regions of 150 patients (68 men, 82 women; mean age 35 ± 16 years). All patients had a FBN1 mutation and underwent dural magnetic resonance imaging. Age was <16 years in 20, 16-25 in 27, 26-35 in 67, and >35 in 36 patients. Prevalence of dural...

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Source

Identifiers

PMID: 23991918
DOI: 10.1111/cge.12264

Genes

FBN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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