Literature DB >> 19299137

A Chinese pedigree of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): clinical and radiological features.

D M Zheng1, F F Xu, Y Gao, H Zhang, S C Han, G R Bi.   

Abstract

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a rare hereditary cerebral vascular disease thought to be confined to Japan. This paper reports a Chinese pedigree of CARASIL in which two patients exhibited all of the typical clinical features of the disease. The radiological features are also discussed and compared with those of CADASIL. These cases illustrate the unique clinical and radiological features of CARASIL and challenge the idea that CARASIL is limited to the Japanese population.

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Year:  2009        PMID: 19299137     DOI: 10.1016/j.jocn.2008.08.031

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  3 in total

1.  A novel mutation in the HTRA1 gene identified in Chinese CARASIL pedigree.

Authors:  Xiao-Ling Wang; Chuan-Fen Li; Hong-Wei Guo; Bing-Zhen Cao
Journal:  CNS Neurosci Ther       Date:  2012-08-20       Impact factor: 5.243

2.  Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.

Authors:  Ilaria Di Donato; Silvia Bianchi; Gian Nicola Gallus; Alfonso Cerase; Ilaria Taglia; Francesca Pescini; Serena Nannucci; Carla Battisti; Domenico Inzitari; Leonardo Pantoni; Andrea Zini; Antonio Federico; Maria Teresa Dotti
Journal:  CNS Neurosci Ther       Date:  2017-08-06       Impact factor: 5.243

3.  Single gene disorders associated with stroke: a review and update on treatment options.

Authors:  Hurmina Muqtadar; Fernando D Testai
Journal:  Curr Treat Options Cardiovasc Med       Date:  2012-06
  3 in total

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