BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is a systemic
hereditary disorder characterized by bilateral diffuse renal cysts. Extrarenal involvement is a …

Background and objectives: Autosomal dominant polycystic kidney disease is a systemic
disorder with a wide range of extrarenal involvement. The scope of this study was to analyze …

Objectives. To assess the prevalence of cysts in the epididymis, seminal vesicles, prostate,
and testes of patients with autosomal dominant polycystic kidney disease (ADPKD) and …

Discussion The association between polycystic kidney disease and infertility due to
dilatation of seminal vesicles is an important, although often unrecognized, cause of …

Adult polycystic kidney disease (APKD) is associated with cyst formation in the kidney, liver,
pancreas, esophagus, ovary, uterus, and brain. Four patients with APKD (aged 45-65 years) …

Retrospective analysis of 99 male autosomal dominant polycystic kidney disease (ADPKD)
patients compared to an age-matched control population showed seminal vesicle ectasia> …

Extrarenal cysts occur in patients with autosomal dominant polycystic kidney disease
(ADPKD) most frequently in the liver. Ovarian cysts have been reported in women with …

Autosomal dominant polycystic kidney disease (ADPKD) is a frequently occurring inherited
condition with cysts in many organs including the kidneys. However, a combination of …

Adult polycystic kidney disease (APKD) is one of the most common inherited disorders
affecting one in 800–1000 live births. Extra‐renal manifestation of APKD is not uncommon …

OBJECTIVE: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by
the presence of multiple cysts in both kidneys. Symptoms of the disease may arise either …