End-stage renal disease in polycystic kidney disease

2013 ◽  
pp. 164-174
Author(s):  
Ahsan Alam ◽  
Ronald D Perrone
Keyword(s):  
Kidney Disease ◽  
Renal Disease ◽  
Polycystic Kidney Disease ◽  
End Stage Renal Disease ◽  
Polycystic Kidney ◽  
Stage Renal Disease ◽  
End Stage

Diagnosis of infected kidney cysts in patients with autosomal dominant polycystic kidney disease and end-stage renal disease

Urologiia ◽  
2021 ◽  
Vol 3_2021 ◽  
pp. 50-55
Author(s):  
A.E. Lubennikov Lubennikov ◽  
A.A. Shishimorov Shishimorov ◽  
R.N. Trushkin Trushkin ◽  
T.K. Isaev T ◽  
O.N. Kotenko Kotenko ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Renal Disease ◽  
Polycystic Kidney Disease ◽  
End Stage Renal Disease ◽  
Autosomal Dominant ◽  
Polycystic Kidney ◽  
Kidney Cysts ◽  
Autosomal Dominant Polycystic Kidney ◽  
Stage Renal Disease ◽  
End Stage

LAPAROSCOPIC NEPHRECTOMY FOR ADULT POLYCYSTIC KIDNEY DISEASE PATIENTS WITH END STAGE RENAL DISEASE

1999 ◽  
pp. 22
Author(s):  
Cathy K. Naughton ◽  
Abdelhamid M. Elbahnasy ◽  
Matthew D. Dunn ◽  
Ralph V. Clayman ◽  
Arieh L. Shalhav ◽  
...  
Keyword(s):  
Kidney Disease ◽  
Renal Disease ◽  
Polycystic Kidney Disease ◽  
End Stage Renal Disease ◽  
Laparoscopic Nephrectomy ◽  
Polycystic Kidney ◽  
Adult Polycystic Kidney Disease ◽  
Stage Renal Disease ◽  
End Stage

scholarly journals Prevalence, risk factors and disease knowledge of polycystic kidney disease in Pakistan

2020 ◽  
Vol 34 ◽  
pp. 205873842096608
Author(s):  
Rabia Zahid ◽  
Muhammad Akram ◽  
Ejaz Rafique
Keyword(s):  
Family History ◽  
Kidney Disease ◽  
Renal Disease ◽  
Polycystic Kidney Disease ◽  
End Stage Renal Disease ◽  
Positive Family History ◽  
Polycystic Kidney ◽  
Surgical Interventions ◽  
Stage Renal Disease ◽  
End Stage

Polycystic kidneys disease refers to cyst(s) formation in kidneys with severe consequences of end stage renal disease thus have higher mortality. It is a common genetic disease occurring either as autosomal dominant polycystic kidney (ADPKD) or autosomal recessive polycystic kidney disease (ARPKD) with prevalence rates of 1/1000 and 1/40,000 respectively. Dominant forms presenting in later (>30) while recessive in earlier ages (infancy) and affecting both sexes and almost all race. The patient experiences many renal as well as extra-renal manifestations with marked hypertension and cyst formation in other organs predominantly in liver. Due to genetic basis, positive family history is considered as major risk factor. Ultrasonography remains the main stay of diagnosis along with family history, by indicating increased renal size and architectural modifications. Initially disease remains asymptomatic, later on symptomatic treatment is suggested with surgical interventions like cyst decortications or drainage. Dialysis proved to be beneficial in end stage renal disease. However renal transplantation is the treatment of choice.

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