1、

Diagnostic value of immunohistochemical study of type ⅳ collagen α 3 and α 5 chains on patients with hereditary nephritis

Ⅳ型胶原α3、α5链免疫组化检测在遗传性肾炎诊断中的意义

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2、

Hereditary nephritis ( alport's syndrome)& on an of pedigree

遗传性肾炎(Alport综合征)&一个家系的调查报告

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3、

Make a special effort to analysis chinical feature, the discussed inheritance patter and diagnosis indication rapid of hereditary nephritis in article.

本文着重分析遗传性肾炎的临床表现,就其早期诊断线索和遗传方式提出讨论。

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4、

This is a type of hereditary nephritis known as Alport's syndrome in which patients may also manifest nerve deafness and eye problems.

名为Alport综合征的遗传性肾炎。病人通常表现为神经性耳聋及眼病。

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5、

RESULTS Three types of abnormal distribution of renal type ⅳ collagen α 3 and α 5 chains were observed in 10 of the 49 patients with hereditary nephritis.

结果:抗α3和α5链的抗体荧光染色在10例患者的肾组织中分布异常,并呈现三种类型。

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6、

METHODOLOGY This study included 49 patients who satisfied the clinical criteria for the diagnosis of hereditary nephritis. Type ⅳ collagen α 3 and α 5 chains in renal biopsy sections were detected with indirect immunofluorescence assay.

方法:采用特异性抗Ⅳ型胶原α3和α5链NC1区域的单克隆抗体,对4例正常人及43例临床疑诊为遗传性肾炎患者的肾脏组织进行了间接免疫荧光染色。

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