ea0015p156 | Diabetes, metabolism and cardiovascular | SFEBES2008
Williams Sian
, Reed Anita
, Reilly Jennifer
, Karet Fiona
, Lhotta Karl
, Strehlau Juergen
, Turner Neil
, Thakker Rajesh
Familial Juvenile Hyperuricaemic Nephropathy (FJHN) is an autosomal dominant disorder that is associated with gout and progressive renal failure. FJHN in 43 families has been reported to be caused by mutations in the UMOD gene, which encodes Uromodulin, also known as the Tamm-Horsfall Glycoprotein, and two families have been reported to have mutations in the transcription factor Hepatocyte Nuclear Factor 1β (HNF-1β), mutations of which usually cause maturity-o...