Wolcott-Rallison syndrome

Wolcott-Rallison syndrome (WRS) is a very rare genetic disease, characterized by permanent neonatal diabetes mellitus (PNDM) with multiple epiphyseal dysplasia and other clinical manifestations, including recurrent episodes of acute liver failure.

Also known as: WRS, Wolcott-Rallison syndrome, early-onset diabetes mellitus with multiple epiphyseal dysplasia, IDDM-MED syndrome, Iddm-Med syndrome, MED-IDDM syndrome, Med-Iddm syndrome, Wolcott Rallison syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Wolcott-Rallison syndrome itself.