遗传性肾病

常染色体显性多囊肾病（Autosomaldominantpolycystickidneydisease，ADPKD）是最常见的威胁人类健康与生命的遗传性肾病，发病率约为1‰-2‰。

Autosomal dominant polycystic kidney disease is one of the most common human fatal hereditary renal diseases with a morbidity of 1 % o ~ 2 % o.

皮肤及肾组织Ⅳ型胶原α链测定在早期诊断遗传性肾病的意义

Significance of epidermal tissue α chains of ⅳ collagen detection in early diagnosis of hereditary nephropathy

方法首次报道国内3例遗传性IgM肾病。

Methods Three patients with hereditary IgM glomerulopathy were report first time in China .

遗传性IgM肾病一家系三例报告及文献复习

Hereditary IgM nephropathy : report of three cases in a kindred and review of literatures

目的加强对遗传性IgM肾病的认识。

Objective To recognize hereditary IgM glomerulopathy .

目的探讨颅内动脉瘤（ICA）与多囊肝肾病即常染色体显性遗传性多囊肾病（ADPKD）的关系。

Objective To explore the relationship of intracranial aneurysm ( ICA ) and autosomal dominant polycystic kidney disease ( ADPKD ) .

目的分析遗传性血尿肾病耳聋综合征（Alportsyndrome，As）病人的听功能改变特点，畸变产物耳声发射（DPOAEs）测试的意义。

Objective To analyze the altered features of auditory functions of hereditary nephritis-nerve deafness syndrome ( Alport syndrome , As ) patients and the significance of distortion product otoacoustic emissions ( DPOAEs ) test .

目的：观察重组人肝细胞生长因子（rhHGF）对常染色体显性遗传性多囊肾病（ADPKD）囊肿衬里上皮细胞合成细胞外基质（ECM）、基质金属蛋白酶及其抑制剂的作用。

Objective : To study the effects of recombinant human hepatocyte growth factor ( rhHGF ) on the synthesis of extracellular matrix ( ECM ) and matrix metalloproteinases and tissue inhibitor of metalloproteinases in autosomal dominant polycystic kidney disease ( ADPKD ) cyst lining epithelial cells .

常染色体显性遗传性多囊肾病研究的热点问题

Hot issues in current research of autosomal dominant polycystic kidney disease

常染色体隐性遗传性多囊肾病：临床、病理与影像学表现

Autosomal recessive polycystic kidnay disease : clinical , pathological and radiological correlations

271例常染色体显性遗传性多囊肾病患者临床分析

Analysis of clinical characteristics of 271 patients with autosomal dominant polycystic kidney disease

2型常染色体显性遗传性多囊肾病致病基因突变研究

Detection of the mutations of autosomal dominant polycystic kidney disease gene 2 in Chinese

西罗莫司延缓肾功能不全常染色体显性遗传性多囊肾病大鼠的疾病进程

Sirolimus slows down disease progression in rats with autosomal dominant polycystic kidney disease and renal dysfunction

目的：观察经后腹腔镜肾囊肿去顶减压术治疗常染色体显性遗传性多囊肾病的临床效果。

Objective : To observe the clinical effect of laparoscopic renal cyst decortication in patients with autosomal dominant polycystic kidney disease .