These recommendations were systematically developed on behalf of the Network for Early
Onset Cystic Kidney Disease (NEOCYST) by an international group of experts in autosomal …

Context Autosomal dominant polycystic kidney disease (ADPKD) is a common disorder that
can cause hypertension during childhood, but the true prevalence of hypertension during …

Autosomal-dominant polycystic kidney disease in infancy and childhood: Progression and
outcome. Background The natural history of autosomal-dominant polycystic kidney disease …

Autosomal dominant polycystic kidney disease (ADPKD) affects 1 in 400 to 1,000 live births,
making it the most common monogenic cause of renal failure. Although no definite cure is …

Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive
polycystic kidney disease (ARPKD) are important inherited kidney diseases with distinct …

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent cause of
genetic renal disease and accounts for 6–10% of patients on renal replacement therapy …

The use of prenatal ultrasonography has resulted in increased numbers of fetuses being
diagnosed with autosomal dominant polycystic kidney disease (ADPKD), but the long-term …

A number of syndromic disorders have renal cysts as a component of their phenotypes.
These disorders can generally be distinguished from autosomal dominant polycystic kidney …

Autosomal dominant polycystic kidney disease in childhood: A longitudinal study. One
hundred fifty–four children aged eighteen years or younger from 83 families with autosomal …

MIM 263200) is a severe, typically early-onset form of cystic disease that primarily involves
the kidneys and biliary tract. Phenotypic expression and age at presentation can be quite …