| Literature DB >> 11757773 |
T Murakami1, K Iwatsuki, T Hayashi, K Sato, E Matsubara, I Nagano, Y Manabe, M Shoji, K Abe.
Abstract
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare hereditary disease characterized by recurrent transient ischemic attacks (TIA) and strokes, and vascular dementia with Notch3 gene mutations as the cause of the disease. To date, there are only a few Japanese families ever reported with a mutation in the gene. Here, we report two more Japanese CADASIL families carrying a missense mutation in the Notch3 gene (R141C) with a unique lesion in the corpus callosum. This is the first report of two unrelated Japanese CADASIL families with a R141C mutation in the Notch3 gene. Although the disease is very rare among the Japanese population, our result suggests a possible relationship of this particular mutation (R141C) with the lesions of the corpus callosum.Entities:
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Year: 2001 PMID: 11757773 DOI: 10.2169/internalmedicine.40.1144
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271