Purpose: Familial renal glucosuria (FRG, OMIM #233100) is a rare but relatively benign genetic condition characterized by persistent isolated glucosuria with a normal blood glucose level. We report three additional SLC5A2 mutations and examine their phenotypic and genetic...
Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced by mutations of the PKD1 and PKD2 genes. PKD1 is located on ...
Endoscopic subureteral injection for treatment of vesicoureteral reflux (VUR) is known to be safe and efficient due to its minimal invasive nature. Being non-migratory, non-antigenic, and biocompatible, Macroplastique (Polydimethylsiloxane) is likely to be stable over time. A 5-...
Nutcracker syndrome is a phenomenon that the left renal vein (LRV) is pressed between the superior mesenteric artery (SMA) and the aorta. Clinical characteristics include gross or microscopic hematuria, orthostatic proteinuria, abdominal pain, and back pain. It occurs due to LRV...
If anyone registers his/her email address, he or she will receive the email of notification when new paper is published in the web site of Child Kidney Dis. Since it is open access journal, the full text is freely available.
Please Sign up.
To submit a manuscript, please visit the Child Kidney Dis e-submission management system at esubmit, read the Instructions for Authors, and log into the Child Kidney Dis e-submission system. For assistance with manuscript submission, please contact: ckdeditor@kspn.org.
Free archive
Anyone may access any past or current articles without logging in.
Manuscript Submission