Table 2 lists the investigations used in assessing ADPKD patients. New unified diagnostic
ultrasound criteria for at-risk PKD1 and PKD2 individuals have recently been reported …

The initial step in diagnosing ADPKD is renal ultrasound. The presence of at least three
unilateral or bilateral renal cysts in patients aged 15 to 39 years and of two cysts in each …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited
cause of kidney failure and accounts for∼ 5% of ESRD population in the United States. The …

Autosomal-dominant polycystic kidney disease (ADPKD) is the most common Mendelian
disorder of the kidney and accounts for approximately 5% of end-stage renal disease in …

United States, occurring in approximately one in every 400 to 1000 live births. 1 ADPKD
accounts for approximately 5 to 10% of end-stage renal failure in the United States requiring …

PURPOSE: To estimate the sensitivity and specificity of ultrasonography (US) in the
diagnosis of autosomal dominant polycystic kidney disease (ADPKD) types 1 and 2, as …

Using age-and height-adjusted total kidney volume, the Mayo Clinic Imaging Classification
provides a validated approach to assess the risk of chronic kidney disease (CKD) …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common Mendelian
disorder of the kidney and affects all racial groups worldwide. It is characterized by focal …

Disease characteristics. Autosomal dominant polycystic kidney disease (ADPKD) is
generally a late-onset, multisystem disorder characterized by bilateral renal cysts; cysts in …

The absence of a positive family history (PFH) in 10%–25% of patients poses a diagnostic
challenge for autosomal dominant polycystic kidney disease (ADPKD). In the Toronto …