Mutational analysis of PKD1 gene in a Chinese family with autosomal dominant polycystic kidney disease

作者：Liu, Jingyan; Li, Lanrong; Liu, Qingmin^*

来源：International Journal of Clinical and Experimental Pathology, 2015, 8(10): 13289-13292.

• Autosomal dominant polycystic kidney disease
• PKD1
• mutational analysis
• Chinese family

Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease and common renal disease. Mutations of PKD genes are responsible for this disease. We analyzed a large Chinese family with ADPKD using Sanger sequencing to identify the mutation responsible for this disease. The family comprised 27 individuals including 10 ADPKD patients. These ADPKD patients had severe renal disease and most of them died very young. We analyzed 6 survival patients gene and found they all had C10529T mutation in exon 35 of PKD1 gene. We did not found gene mutation in any unaffected relatives or 300 unrelated controls. These findings suggested that the C10529T mutation in PKD1 gene might be the pathogenic mutation responsible for the disease in this family.

• 出版日期2015
• 单位山东大学; 临沂市人民医院; 山东省立医院