期刊论文详细信息
BMC Nephrology
Autosomal dominant polycystic kidney disease with ectopic unilateral multicystic dysplastic kidney
Chang-Lin Mei3  Wei-Ping Jia2  Cong-Rong Wang2  Chen-Ming Xu1  He-Feng Huang1  Zhi-Guo Mao3  Dong-Ping Chen3  Jing Xu3 
[1] Zhejiang University affiliated Gynecology and Obstetrics Hospital, Key Laboratory of Reproductive Genetics, Zhejiang University, Hangzhou, China;Division of Endocrinology, Shanghai Diabetes Institute, Shanghai Sixth People’s Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China;Division of Nephrology, Kidney Institute of CPLA, Changzheng Hospital, Second Military Medical University, 415 Fengyang Rd, 200003, Shanghai, China
关键词: Unilateral;    Multicystic dysplasia;    Ectopia;    Autosomal dominant polycystic kidney disease;   
Others  :  1083000
DOI  :  10.1186/1471-2369-14-38
 received in 2012-11-04, accepted in 2013-02-13,  发布年份 2013
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【 摘 要 】

Background

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disorder. In most cases, ADPKD similarly affects bilateral kidneys.

Case presentation

Among the 605 ADPKD patients that were followed up by our center, we identified two male patients with unilateral ADPKD. The cases were remarkable because the patients also had ectopia and multicystic dysplasia in the contralateral kidney, which are generally sporadic disease conditions. Both patients tested positive for polycystic kidney disease 1 mutation, but negative for hepatocyte nuclear factor 1 beta mutation. Moreover, the deterioration of their kidney function seemed to be quicker than their age- and sex-matched controls and siblings. Both patients had started a long-term hemodialysis in their 40s.

Conclusion

Anatomical and genetic abnormality in patients with ADPKD may be more frequent and complex than previously believed. The compensatory capacity in patients with ADPKD is fragile, and missing one kidney could accelerate the deterioration of renal function.

【 授权许可】

   
2013 Xu et al; licensee BioMed Central Ltd.

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