HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene.

Abstract
After renal transplantation for congenital cystic kidney disease of unknown origin, a 14-year-old boy, who was previously normoglycemic, had "steroid-induced" diabetes mellitus, which was treated with insulin. Transplant failure from chronic rejection and subsequent transplant nephrectomy allowed discontinuation of corticosteroids, the gradual withdrawal of insulin and normoglycemia. The recent description of renal cysts and diabetes (RCAD) syndrome and a strong paternal family history of early-onset diabetes mellitus prompted genetic screening of the hepatocyte nuclear factor-1beta gene. A novel heterozygous frameshift mutation in exon 1 was identified, adding to the 12 kindreds thus far described. This case highlights the unmasking of the hyperglycemic component of the RCAD syndrome in the immediate postoperative period after renal transplantation and emphasizes the pleiotropic manifestations of this important genetic kidney disease.
AuthorsSimon C Waller, Lesley Rees, Adrian S Woolf, Sian Ellard, Ewan R Pearson, Andrew T Hattersley, Coralie Bingham
JournalAmerican journal of kidney diseases : the official journal of the National Kidney Foundation (Am J Kidney Dis) Vol. 40 Issue 6 Pg. 1325-30 (Dec 2002) ISSN: 1523-6838 [Electronic] United States
PMID12460054 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2002 by the National Kidney Foundation, Inc.
Chemical References
  • DNA-Binding Proteins
  • HNF1B protein, human
  • Transcription Factors
  • Hepatocyte Nuclear Factor 1-beta
  • DNA
Topics
  • Adolescent
  • Cysts (blood, diagnosis, diagnostic imaging, genetics)
  • DNA (blood)
  • DNA Mutational Analysis (methods)
  • DNA-Binding Proteins (genetics)
  • Diabetes Mellitus (blood, genetics)
  • Exons (genetics)
  • Frameshift Mutation (genetics)
  • Genetic Carrier Screening
  • Hepatocyte Nuclear Factor 1-beta
  • Humans
  • Hyperglycemia (blood, genetics)
  • Kidney Diseases (blood, diagnosis, diagnostic imaging, genetics)
  • Kidney Transplantation (adverse effects)
  • Leukocytes (chemistry)
  • Male
  • Prenatal Diagnosis (methods)
  • Syndrome
  • Transcription Factors (genetics)
  • Ultrasonography

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: