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Up to: Syndromic disease · Autosomal recessive disease · Spondyloepiphyseal dysplasia
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.
This condition has no sub-types.