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Six year old with autoimmune polyglandular syndrome: Can genetics tell us the story?

  • Steven Ghanny
  • , Robert Wallerstein
  • , Amy Chartoff
  • , Janet Post
  • , Javier Aisenberg
  • , Valerie Auyeung
  • Santa Clara Valley Medical Center
  • HACKENSACK UNIVERSITY MEDICAL CENTER

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

Children who have diabetes mellitus type 1 (DMT1) are at increased risk of developing other autoimmune diseases. These associated diseases include Hashimoto's thyroiditis, Graves' disease, Celiac disease, and Addison's disease. Since Addison's disease is potentially fatal if undiagnosed and untreated, it would be prudent to effectively screen individuals to determine if they are at risk of developing this disease. We present a case of a 6 year old male with a history of DMT1, who presented in adrenal crisis and was subsequently diagnosed with Addison's disease. HLA-DRB1 404/DR4 is one of the genes involved in the development of Addison's disease in children with DMT1. Our patient later tested positive for this haplotype. Genetic testing is not routinely done in patients with (DMT1) to determine if they will potentially develop other associated conditions. We propose using genetic testing of associated HLA haplotypes to screen children with DMT1 for Addison's disease.

Original languageEnglish
Pages (from-to)725-728
Number of pages4
JournalJournal of Pediatric Endocrinology and Metabolism
Volume23
Issue number7
DOIs
StatePublished - 2010

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Addison's disease
  • Autoimmune polyglandular syndrome
  • Screening
  • Type 1 DM

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