Literature DB >> 8697929

[Systemic manifestations of adult polycystic kidney disease: an analysis of 205 cases].

Y Liu1, H Zhang, H Zhong.   

Abstract

Adult polycystic kidney disease (APKD) is a common genetic disease and one of the important reasons of end stage renal failure. Although renal multiple cysts are clearly an important manifestation of APKD; other systemic manifestations are both common and clinically important. The authors reviewed 205 cases from 180 APKD families (107 male 98 female). Their age ranged from 10 to 71 years. Renal cyst is one of the many renal manifestations. Hypertension, hematuria and flank pain are its major complications. Hepatic cysts, pancreatic cysts, cardiac valvular lesions, intracranial aneurysms and splenic cysts are included in the array of systemic manifestations.

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Mesh:

Year:  1995        PMID: 8697929

Source DB:  PubMed          Journal:  Zhonghua Nei Ke Za Zhi        ISSN: 0578-1426


  3 in total

Review 1.  Thoracic aortic dissection in a patient with autosomal dominant polycystic kidney disease.

Authors:  T Adeola; O Adeleye; J L Potts; M Faulkner; A Oso
Journal:  J Natl Med Assoc       Date:  2001 Jul-Aug       Impact factor: 1.798

2.  RAPID-ADPKD (Retrospective epidemiological study of Asia-Pacific patients with rapId Disease progression of Autosomal Dominant Polycystic Kidney Disease): study protocol for a multinational, retrospective cohort study.

Authors:  Hyunjin Ryu; Hayne C Park; Yun Kyu Oh; Irene Sangadi; Annette Wong; Changlin Mei; Tevfik Ecder; Angela Yee-Moon Wang; Tze-Wah Kao; Jenq-Wen Huang; Gopala K Rangan; Curie Ahn
Journal:  BMJ Open       Date:  2020-02-06       Impact factor: 2.692

Review 3.  The Clinical Manifestation and Management of Autosomal Dominant Polycystic Kidney Disease in China.

Authors:  Cheng Xue; Chen-Chen Zhou; Ming Wu; Chang-Lin Mei
Journal:  Kidney Dis (Basel)       Date:  2016-10-06
  3 in total

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