alport

Early Diagnosis of Alport ′ s Syndrome in 5 Children and Literature Reviews

早期诊断Alport′s综合征5例及文献复习

Clinical and Audiological Features Hearing Loss in Patients With Alport Syndrome

Alport综合征的临床及听力学表现

Features of phenotype and genotype in Chinese Alport syndrome patients

中国Alport综合征表型和基因型特征

Ultrastructural pathologic diagnosis of thin glomerular basement membrane disease and Alport syndrome

肾小球薄基底膜病及遗传性肾炎的超微病理诊断

Objective To assess the clinical manifestation of Alport syndrome , especially the ocular features .

目的总结Alport综合征的临床表现，尤其是眼部特征。

Alport syndrome & an analysis of 22 families

Alport综合征22个家系临床病理分析

The significance of collagen ⅳ α chain expression on basement membrane in patients with Alport syndrome

Alport综合征基膜Ⅳ型胶原α链表达异常的临床意义

Clinical pathology of Alport 's syndrome in children

小儿Alport综合征的临床病理分析

Pedigree investigation and immunohistochemical study of autosomal dominant alport syndrome

常染色体显性遗传Alport综合征的家系调查及免疫组化研究

Distortion product otoacoustic emission test in Alport syndrome

Alport综合征畸变产物耳声发射测试

Relationship between genotype and phenotype in Alport syndrome : analysis at α 5 (ⅳ) chain mRNA level

从α5（Ⅳ）链mRNA突变分析看Alport综合征基因型和表型关系

Relationship between the distribution features of type ⅳ collagen α chains and the clinical phenotype in Alport syndrome

Alport综合征Ⅳ型胶原分布特点及其与临床表型的联系

Objective : To evaluate the significance of electron-microscopy in the diagnosis of children Alport syndrome .

目的：评价电镜检查对小儿遗传性进行性肾炎的诊断意义。

A clinicopathological study of Alport syndrome and detection of type ⅳ collagen chains in Alport patients

Alport综合征临床病理研究及基底膜Ⅳ型胶原检测

Detection of type ⅳ collagen α chains in basement membranes for determining the hereditary modes of Alport syndrome

检测不同组织基底膜IV型胶原α链确定Alport综合征遗传型

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

Correlation between ultrastructural changes of glomerular basement membrane and abnormal distribution of laminins in patients with Alport 's syndrome

Alport综合征患者肾小球基底膜超微结构改变与层粘连蛋白的异常分布

Quantitative analysis of type ⅳ collagen alpha 3 and alpha 5 chain in the glomerular basement membrane in patients with Alport syndrome

肾小球基膜Ⅳ型胶原亚链定量分析在Alport综合征诊断中的意义

Membranoproliferative glomerulonephritis ? Alport syndrome and minimal change were the same 6 cases ( 5.5 % );

膜增生性肾炎、Alport综合征及微小病变各6例（5.5%）；

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。

As in normal kidney , Alport kidney revealed similar staining for the laminin α 5 and γ 1 chains .

层粘连蛋白α5、γ1链在AS患者和其他肾脏病组织沉积同正常肾组织。

METHODS : 7 eyes from 4 patients with Alport syndrome underwent phacoemulsification with IOL implantation due to anterior lenticonus .

方法：Alport综合征患者4例，7眼因前圆锥晶状体行超声乳化联合IOL植入手术。

Objective To analyze type IV collagen a5 chain mRNA and to study the relationship between genotype and phenotype in X-linked Alport syndrome .

目的检测分析X连锁型Alport综合征（AS）患者α5（Ⅳ）链mRNA及其序列并探讨其基因型与表型之间的关系。

CONCLUSION : We recommend the phacoemulsification with IOL implantation as a safe procedure in anterior lenticonus due to Alport syndrome .

结论：我们认为对于前圆锥晶状体伴有Alport综合征患者采用超声乳化联合IOL植入手术治疗，是一种安全的疗法。

Objective To make the diagnosis and identify the hereditary type of an Alport syndrome ( AS ) patient by pedigree investigation , renal biopsy analysis and immunohistochemical study .

目的通过对一Alport综合征患者的家系调查、肾活检分析及免疫组化研究，明确其临床诊断，确定其遗传方式。

Screening for the mutations of COL4A3 / COL4A4 genes in an autosomal recessive Alport syndrome family

常染色体隐性遗传Alport综合征一家系COL4A3及COL4A4基因突变分析

Objective To identify the distribution of the laminin α 5 ,α 2 and γ 1 chains within renal basement membrane in Alport syndrome ( AS ) .

目的观察Alport综合征（AS）患者肾组织层粘连蛋白α2链、α5链和γ1链的分布。

Objective To explore the expression of different α chains of type ⅳ collagen on basement membranes for determining the hereditary modes of Alport syndrome ( AS ) in Chinese patients .

目的探讨中国人不同遗传型Alport综合征（AS）患者基底膜α链的表达及其在判断遗传型方面的应用。

AIM : We describe visual improvement after phacoemulsification with intraocular lens ( IOL ) implantation in 7 eyes with anterior lenticonus secondary to Alport syndrome .

目的：观察超声乳化联合IOL植入治疗7眼前圆锥晶状体伴有Alport综合征患者的手术效果。

Alport syndrome ( AS ) is a hereditary kidney disease associated with extrarenal complications , such as sensorineural deafness and eye abnormalities and so on .

Alport综合征又称遗传性肾炎，患者往往并发肾外综合征，如神经性耳聋和眼疾等。