Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy

Eur J Pediatr. 2000 Aug;159(8):631-3. doi: 10.1007/pl00008394.

Abstract

Clinical analysis and genetic investigations of new cases of Wolcott-Rallison syndrome are needed to evaluate the role of the gene(s) directly or indirectly implicated in pancreas development and in the aetiology of the syndrome.

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / diagnosis*
  • Abnormalities, Multiple / genetics*
  • Child
  • Diabetes Mellitus, Type 1 / diagnosis*
  • Diabetes Mellitus, Type 1 / genetics*
  • Dwarfism / diagnosis*
  • Dwarfism / genetics*
  • Exocrine Pancreatic Insufficiency / diagnosis*
  • Exocrine Pancreatic Insufficiency / genetics*
  • Female
  • Humans
  • Karyotyping
  • Osteochondrodysplasias / diagnosis*
  • Osteochondrodysplasias / genetics*
  • Syndrome