Article
New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation.
Pediatric transplantation - 1 May 2016
Kanda Shoichiro, Morisada Naoya, Kaneko Naoto, Yabuuchi Tomoo, Nawashiro Yuri, Tada Norimasa, Nishiyama Kei, Miyai Takayuki, Sugawara Noriko, Ishizuka Kiyonobu, Chikamoto Hiroko, Akioka Yuko, Iijima Kazumoto, Hattori Motoshi
Abstract excerpt
CAKUT are the most frequent causes of ESRD in children. Mutations in the gene encoding HNF1B, a transcription factor involved in organ development and maintenance, cause a multisystem disorder that includes CAKUT, diabetes, and liver dysfunction. Here, we describe the case of a patient with renal hypodysplasia who developed NODAT presenting with liver dysfunction. The NODAT was initially thought to be steroid and...
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