hereditary nephritis

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。

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

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。

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。

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。

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