Recent advances in studies on autosomal dominant adult polycystic kidney disease

Adult polycystic kidney disease (APKD) is a severe autosomal dominant inheritable renal disease with high incidence. Because of the late-onset of the disease, patients might have transferred the disease gene to the next generation when diagnosis is made. Since its pathogenic molecular mechanism is still not completely clear and the shortage of effective medicines, the prevention and treatment of the disease is still not satisfactory. In the present article, the recent advances in the research on the pathogenesis, gene diagnosis and management of APKD are reviewed.

Medienart:

E-Artikel

Erscheinungsjahr:

2010

Erschienen:

2010

Enthalten in:

Zur Gesamtaufnahme - volume:27

Enthalten in:

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 27(2010), 4 vom: 27. Aug., Seite 402-5

Sprache:

Chinesisch

Beteiligte Personen:

Yu, Chao-wen [VerfasserIn]
Zhang, Si-zhong [VerfasserIn]

Links:

Volltext

Themen:

English Abstract
Journal Article
TRPP Cation Channels

Anmerkungen:

Date Completed 10.12.2010

Date Revised 02.08.2010

published: Print

Citation Status MEDLINE

doi:

10.3760/cma.j.issn.1003-9406.2010.04.009

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM200009176