Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant
disorder in pediatric nephrology. This genetic disease is mainly caused by variants in the …

Autosomal recessive polycystic kidney disease–PKHD1 (ARPKD-PKHD1) is characterized
by primary involvement of the kidneys and liver with mostly secondary effects seen in other …

In pediatric kidney failure, native kidneys may pose a risk to successful transplant outcomes.
The indications and timing of native nephrectomy represent a controversial management …

There are no clinical guidelines for performing nephrectomy in patients with autosomal
recessive polycystic kidney disease (ARPKD). Few reports have described the clinical …

Background Autosomal recessive polycystic kidney disease (ARPKD) is a significant cause
of morbidity and mortality in infants and children. In severe cases bilateral nephrectomies …

Autosomal recessive polycystic kidney disease (ARPKD) is a monogenic disorder that
primarily involves mutations in the PKHD1 gene, although rare, atypical forms of ARPKD …

We read with great interest the article by Overman RE and colleagues [1] describing their
experience in performing early nephrectomies in neonates with symptomatic autosomal …

Sažetak Nefrektomija, kirurški postupak uklanjanja bubrega, kirurški je zahvat koji se
razvijao od prvih fizioloških eksperimenata na životinjama do današnjih rutinskih uroloških …

INTRODUCTION—Autosomal recessive polycystic kidney disease (ARPKD, MIM# 263200),
previously called infantile polycystic kidney disease, is a recessively inherited disorder …

Clinical characteristics Autosomal recessive polycystic kidney disease–PKHD1 (ARPKD-
PKHD1) is characterized by primary involvement of the kidneys and liver with mostly …