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Recent advances in studies on autosomal dominant adult polycystic kidney disease / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 402-405, 2010.
Article in Chinese | WPRIM | ID: wpr-234396
ABSTRACT
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.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Research / Polycystic Kidney, Autosomal Dominant / TRPP Cation Channels / Genetics Limits: Aged / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Research / Polycystic Kidney, Autosomal Dominant / TRPP Cation Channels / Genetics Limits: Aged / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2010 Type: Article