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Clinical variability of the cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in two siblings of a large family showing the same mutation

Authors Vyshka G, Kruja J

Received 21 July 2013

Accepted for publication 24 August 2013

Published 1 October 2013 Volume 2013:6 Pages 59—63

DOI https://doi.org/10.2147/IMCRJ.S51875

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3


Video abstract presented by Gentian Vyshka

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Gentian Vyshka,1 Jera Kruja2

1Biomedical and Experimental Department, University of Medicine Tirana, 2Neurology Department, Mother Theresa University Hospital Centre, Tirana, Albania

Abstract: A 44-year-old Albanian male was consulted and diagnosed with dementia. His magnetic resonance imaging suggested diffuse white-matter changes. The suspicion of cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) was raised, and a genetic analysis confirmed such a suspicion through uncovering a pathogenic mutation at the level of exon 4 (c.475C>T) of chromosome 19. The patient came from a large family of 13 children, all of whom underwent clinical, genetic, and imaging examination. The pathogenic mutation was found present only in his eldest sister (50 years old), and she presented also very suggestive signs of CADASIL in her respective imaging study, but without any clinically significant counterpart. All other siblings were free from clinical and radiological signs of the disorder. Our opinion was that we were dealing with a mutation showing a very low level of penetrance, with only two siblings affected in a large Albanian family with 13 children.

Keywords: CADASIL, headache, dementia, subcortical infarcts, leukoencephalopathy

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