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听神经瘤的流行病学、发病机制及遗传学

Epidemiology, pathogenesis, and genetics of acoustic tumors.

作者信息

Lanser M J, Sussman S A, Frazer K

机构信息

Department of Otolaryngology-Head and Neck Surgery, University of California, San Francisco 94117-0958.

出版信息

Otolaryngol Clin North Am. 1992 Jun;25(3):499-520.

PMID:1625863
Abstract

This article reviews the epidemiology of both unilateral and bilateral (NF-2) acoustic tumors. The growth rate of acoustic tumors is examined from a clinical, radiographic, and laboratory perspective. The anatomic, histologic, and biochemical considerations as well as the influences of sex hormones on acoustic tumor formation are reviewed. Also presented are an update on the laboratory search for the NF-2 gene on chromosome 22 and recently identified DNA markers. Predictions are made concerning the potential future applications of genetic testing for prenatal or presymptomatic diagnosis of the disease that causes bilateral acoustic tumors.

摘要

本文综述了单侧及双侧(神经纤维瘤病2型)听神经瘤的流行病学。从临床、影像学和实验室角度研究了听神经瘤的生长速率。综述了解剖学、组织学和生物化学方面的因素以及性激素对听神经瘤形成的影响。还介绍了在22号染色体上寻找神经纤维瘤病2型基因的实验室研究进展以及最近鉴定出的DNA标记。对基因检测在导致双侧听神经瘤疾病的产前或症状前诊断中的潜在未来应用进行了预测。

相似文献

1
Epidemiology, pathogenesis, and genetics of acoustic tumors.听神经瘤的流行病学、发病机制及遗传学
Otolaryngol Clin North Am. 1992 Jun;25(3):499-520.
2
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22.双侧听神经纤维瘤病与22号染色体上一个DNA标记的遗传连锁。
Nature. 1987;329(6136):246-8. doi: 10.1038/329246a0.
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Neurofibromatosis 2: clinical and DNA linkage studies of a large kindred.神经纤维瘤病2型:一个大家族的临床及DNA连锁研究
N Engl J Med. 1988 Aug 4;319(5):278-83. doi: 10.1056/NEJM198808043190505.
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[Genetics of neurofibromatosis: recent progress and prospects].[神经纤维瘤病的遗传学:近期进展与展望]
Rev Neurol (Paris). 1991;147(10):644-52.
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Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma.22号染色体上的基因缺失在人类听神经瘤肿瘤发生中的作用
Nature. 1986;322(6080):644-7. doi: 10.1038/322644a0.
6
Early childhood diagnosis of acoustic neuromas in presymptomatic individuals at risk for neurofibromatosis 2.对有患2型神经纤维瘤病风险的无症状个体进行听神经瘤的幼儿期诊断。
Am J Med Genet. 1991 Dec 1;41(3):325-9. doi: 10.1002/ajmg.1320410313.
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Molecular genetics of acoustic tumors.听神经瘤的分子遗传学
Otolaryngol Clin North Am. 1992 Oct;25(5):995-1009.
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Progress towards the isolation and characterization of the genes causing neurofibromatosis.在导致神经纤维瘤病的基因分离与特性鉴定方面取得的进展。
Cancer Surv. 1990;9(4):689-702.
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Management of bilateral acoustic tumors.双侧听神经瘤的管理
Laryngoscope. 1989 May;99(5):475-84. doi: 10.1288/00005537-198905000-00002.
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[Neurofibromatosis: current clinical and molecular genetic aspects from the neurologic viewpoint].[神经纤维瘤病:从神经学角度看当前的临床和分子遗传学方面]
Nervenarzt. 1991 Jun;62(6):340-8.

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