Boy with autosomal recessive polycystic kidney and autosomal dominant polycystic liver disease
Pediatric Nephrology, 04/09/2012
Zingg–Schenk A et al. – The patient with Autosomal recessive polycystic kidney disease (ARPKD) and polycystic liver disease (PCLD) has so far demonstrated a benign clinical outcome, consistent with the great phenotypic variability of ARPKD and, apart from the liver cyst, asymptomatic manifestation of PCLD in childhood.
