Introduction: Describe the surgical sequence in a 55-year-old woman with an Autosomal
Dominant Polycystic Kidney (ADPKD) Case Presentation: We performed three surgical …

Objective: To assess the transplant outcome of patients who underwent concurrent bilateral
nephrectomies (CBN) during kidney transplantation (KT) owing to autosomal dominant …

Abstract Background and Aims At the present, discussions continue on the indications and
timing of performing kidney nephrectomy in patients with autosomal dominant polycystic …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary
kidney disease. It is characterized by progressive cyst formation in both kidneys, often …

Autosomal dominant polycystic kidney disease is a common cause of end-stage renal failure
and an indication for transplant. The genetic mutation in autosomal dominant polycystic …

BACKGROUND: The most frequent genetic disease of the kidneys occurring in 1 of 1000
inhabitants is autosomal-dominant polycystic kidney disease (ADPKD). Growing renal cysts …

Background: End-stage renal failure patients benefit most from kidney transplantation. Due
to big kidneys and organ compression, autosomal dominant polycystic kidney disease …

Polycystic kidney disease is a multisystemic familial inherited disease. A symptomatic
treatment approach is the standard modality for autosomal dominant polycystic kidney …

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the occurrence
of multiple cysts that increase the size of both kidneys, progressively reducing kidney …

Native nephrectomy (NN) in patients with autosomal dominant polycystic kidney disease
(ADPKD) is indicated in cases of recurrent urinary tract infections and hematuria, neoplastic …