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Clinical and genetic characteristics of Korean autosomal dominant polycystic kidney disease patients
The Korean Journal of Internal Medicine ; : 767-779, 2021.
Article in English | WPRIM | ID: wpr-903660
ABSTRACT
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. It is characterized by cyst growth in the kidneys, resulting in kidney enlargement and end-stage kidney disease. The polycystic kidney disease 1 (PKD1) and PKD2 have been identified as genes related to ADPKD and their significance in the molecular pathology of the disease has been studied. A disease-modifying drug has been approved; therefore, it has become important to identify patients at a high risk of kidney disease progression. Genetic tests, image analysis methods, and clinical factors for kidney disease progression prediction have been established. This review describes genetic and clinical characteristics, and discusses ongoing studies in Korean ADPKD patients.
Full text: Available Index: WPRIM (Western Pacific) Type of study: Prognostic study Language: English Journal: The Korean Journal of Internal Medicine Year: 2021 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Type of study: Prognostic study Language: English Journal: The Korean Journal of Internal Medicine Year: 2021 Type: Article