5. The Case Of A Complicated Autosomal Dominant Polycystic Kidney Disease

Authors

  • B.K. Isamatov JSC “National Scientific Center of Surgery named after A.N. Syzganova“, State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan
  • G.M. Adenova State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan
  • D.B. Gebel State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan
  • G.K. Amirov State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan
  • B.Zh. Esenkulov State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan
  • R.A. Gasanov State Clinical Hospital “ The city emergency hospital of Almaty city“ Almaty, Kazakhstan

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Abstract

Autosomal dominant polycystic kidney disease is the most common inherited kidney disease found in adults. The urgency of the problem is due to the peculiarity of the development and growth of cysts, the in-ability of existing methods of treatment to prevent an increase in the size of cysts and kidneys, and progres-sive impaired renal function. This article describes the general characteristics of ADPP, presents an analysis of the clinical case of a complicated course of ADPP.

Keywords

duodenal ulcer, bleeding

References

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Published

2019-12-01

Issue

No. 4 (2019)

Section

Статьи