Different clinical phenotypes in monozygotic CADASIL twins with a novel NOTCH3 mutation.
نویسندگان
چکیده
BACKGROUND AND PURPOSE CADASIL is a hereditary arteriopathy causing recurrent strokes and cognitive decline. Because monozygotic twins have identical genetic background, differences in their environment and lifestyle could reveal factors that may influence CADASIL patients' clinical course, which is highly variable even within the same family. METHODS We describe differences in clinical and imaging findings in a pair of monozygotic CADASIL twins. RESULTS Twin B experienced his first-ever stroke 14 years earlier than twin A, and his symptoms, signs, and imaging findings were more severe. Distinguishing factors were twin B's smoking as well as twin A's physical activity and earlier statin treatment. Causative NOTCH3 mutation was a novel c.752G>A -substitution (p.Cys251Tyr). CONCLUSIONS The phenotypic differences in these monozygotic twins suggest influence of environmental and lifestyle factors on the clinical course of CADASIL.
منابع مشابه
Novel mutation of the notch3 gene in arabic family with CADASIL
Mutations in the NOTCH3 gene are responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), an adult onset hereditary angiopathy leading to ischemic stroke, vascular dementia and psychiatric disorders. All mutation of NOTCH3 described so far are striking stereotyped leading to the gain or loss of cystiene residue in a given epidermal gr...
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عنوان ژورنال:
- Stroke
دوره 40 6 شماره
صفحات -
تاریخ انتشار 2009