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首页> 外文期刊>European neurology >Very high prevalence of right-to-left shunt on transcranial Doppler in an Italian family with cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.
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Very high prevalence of right-to-left shunt on transcranial Doppler in an Italian family with cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.

机译:在患有脑常染色体显性血管病伴皮质下梗死和白脑病的意大利家庭中,经颅多普勒从右向左分流的患病率很高。

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BACKGROUND AND PURPOSE: Cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an autosomal dominant hereditary disease whose clinical expression is a stepwise subcortical vascular dementia. Initial presentation of the disease involves transient or stabilized focal neurological deficits, migraine and mood changes. Recently, a high prevalence of right-to-left shunt (RLS) due to patent foramen ovale has been reported in subjects with migraine. The aim of our study was to determine the prevalence of RLS in CADASIL with and without migraine. METHODS: We performed transcranial Doppler with gaseous contrast in 5 members of an Italian family with CADASIL, diagnosed by means of genetic and skin biopsy criteria. We then compared the prevalence of RLS in 40 consecutive subjects with juvenile stroke, 80 asymptomatic subjects affected by migraine with aura and 50 normal controls. RESULTS: A very high prevalence of RLS was found in CADASIL patients (4/5, 80%), as opposed to young subjects with ischemic stroke (15/40, 37%), asymptomatic subjects with migraine (32/80, 40%) and normal controls (8/50, 16%). All the subjects with CADASIL and migraine (4/4) showed RLS. The difference between CADASIL patients and controls was highly significant (p = 0.006). CONCLUSIONS: We suggest an association between CADASIL and RLS, possibly due to the abnormal development of the endocardial cushion influenced by Notch 3 mutation. Our hypothesis needs to be tested in larger samples. Copyright 2001 S. Karger AG, Basel
机译:背景与目的:脑常染色体显性遗传血管病伴皮质下梗死和白质脑病(CADASIL)是一种常染色体显性遗传病,其临床表现为逐步性皮层下血管性痴呆。该病的最初表现包括短暂或稳定的局灶性神经功能缺损,偏头痛和情绪变化。最近,在偏头痛患者中,由于卵圆孔未闭,从右向左分流(RLS)的发病率很高。我们研究的目的是确定伴或不伴偏头痛的CADASIL中RLS的患病率。方法:我们对意大利CADASIL家族的5名成员进行了经气道造影的经颅多普勒检查,通过遗传学和皮肤活检标准进行诊断。然后,我们比较了40例青少年卒中,80名无症状偏头痛先兆患者和50例正常对照的无症状受试者的RLS患病率。结果:CADASIL患者中RLS的患病率很高(4/5,80%),而年轻的缺血性卒中患者(15/40,37%),无症状的偏头痛患者(32/80,40%) )和正常对照(8 / 50,16%)。所有患有CADASIL和偏头痛(4/4)的受试者均显示RLS。 CADASIL患者与对照组之间的差异非常显着(p = 0.006)。结论:我们建议CADASIL和RLS之间存在关联,可能是由于Notch 3突变影响了心内膜垫的异常发展。我们的假设需要在更大的样本中进行检验。版权所有2001 S. Karger AG,巴塞尔

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