Literature DB >> 20857845

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

Steven Ghanny1, Robert Wallerstein, Amy Chartoff, Janet Post, Javier Aisenberg, Valerie Auyeung.   

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.

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Year:  2010        PMID: 20857845     DOI: 10.1515/jpem.2010.23.7.725

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  1 in total

1.  Polyglandular autoimmune syndrome (PGA)--type 2 with diabetic ketoacidosis.

Authors:  Rakesh Mondal; Sumantra Sarkar; Madhumita Nandi; Indira Banerjee
Journal:  Indian J Pediatr       Date:  2011-10-19       Impact factor: 1.967

  1 in total

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