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常染色体隐性遗传颅内蛛网膜囊肿家系定位于 6q22.31-23.2.

Intracranial arachnoid cyst family with autosomal recessive trait mapped to chromosome 6q22.31-23.2.

机构信息

Department of Neurosurgery, Cumhuriyet University School of Medicine, Kampus, Merkez, Sivas, Turkey, 58140.

出版信息

Acta Neurochir (Wien). 2012 Jul;154(7):1287-92. doi: 10.1007/s00701-012-1312-6. Epub 2012 Mar 3.

Abstract

BACKGROUND

Arachnoid cysts are congenital fluid-filled compartments within the cerebrospinal fluid cisterns and cerebral fissures. They most commonly occur sporadically, and familial occurrence has rarely been reported. In this study, we showed the first genetic linkage in the literature in a pure intracranial arachnoid cyst family with autosomal recessive trait.

METHODS

We identified an intracranial arachnoid cyst family in southern Turkey whose six of seven offspring had intracranial arachnoid cysts in different localizations, and collected venous blood from seven offspring of the family. Whole-genome linkage analysis was performed in all offspring.

RESULTS

A theorical maximum logarithm of the odds score of 4.6 was identified at chromosome 6q22.31-23.2. This result shows strong genetic linkage to this locus.

CONCLUSIONS

We present the first genetic linkage analysis result in a pure intracranial arachnoid cyst family in literature. Further investigation of this linkage area can reveal a causative gene causing the intracranial arachnoid cyst phenotype and can illuminate the pathogenesis of this disease.

摘要

背景

蛛网膜囊肿是脑脊液池和脑裂内先天性充满液体的分隔。它们最常见于散发性,家族性发生很少见。在这项研究中,我们在一个具有常染色体隐性特征的纯颅内蛛网膜囊肿家族中展示了文献中的第一个遗传连锁。

方法

我们在土耳其南部鉴定了一个颅内蛛网膜囊肿家族,其七个后代中的六个在不同部位有颅内蛛网膜囊肿,并从该家族的七个后代中采集静脉血。对所有后代进行全基因组连锁分析。

结果

在染色体 6q22.31-23.2 处鉴定出理论最大对数优势分数为 4.6。这一结果显示与该基因座有强烈的遗传连锁。

结论

我们在文献中提出了第一个纯颅内蛛网膜囊肿家族的遗传连锁分析结果。对该连锁区域的进一步研究可以揭示导致颅内蛛网膜囊肿表型的致病基因,并阐明该疾病的发病机制。

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