IngentaConnect A new de novo Notch3 mutation causing CADASIL

Authors: Coto, E.¹; Menéndez, M.²; Navarro, R.²; García-Castro, M.¹; Alvarez, V.¹

Source: European Journal of Neurology, Volume 13, Number 6, June 2006 , pp. 628-631(4)

Abstract:

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is one of the most common hereditary forms of stroke, and migraine with aura, mood disorders, or dementia, are also frequently found in these patients. Missense mutations in the Notch3 gene that create or destroy cysteine residues, have been found in most cases with a family history of the disease, although a few sporadic cases harbouring Notch3 mutations have also been described. Here, we describe a 44-year-old patient with clinical features of CADASIL who was a carrier of a new Notch3 mutation: cys128→gly. Both parents were alive and healthy, and negative for the mutation. This case illustrates the interest of analysing the Notch3 gene in cases with clinical features of CADASIL, even in the absence of a family history of the disease.

Keywords: CADASIL; mutations; Notch3 gene

Document Type: Research article

DOI: 10.1111/j.1468-1331.2006.01337.x

Affiliations: 1: Genetica Molecular 2: Servicio de Neurologia-Hospital Central de Asturias, Servicio de Salud del Principado de Asturias, Asturias, Spain

The full text electronic article is available for purchase. You will be able to download the full text electronic article after payment.

$50.39 plus tax Refund Policy