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Home > Autoimmune polyendocrine syndrome


 

In medicine, autoimmune polyendocrine syndromes are a heterogenous group of rare diseases characterised by autoimmune activity against more than one endocrine organs, although non-endocrine organs can be affected.

There are three "autoimmune polyendocrine syndromes", and a number of other diseases which have endocrine autoimmunity as one of their features.

1 The syndromes

1.1 Type 1

Autoimmune polyendocrine syndrome, type 1 is also known as the candidiasis- hypoparathyroidism- Addison's disease-syndrome after its main features:

As opposed to type 2, this syndrome inherits in an autosomal recessive fashion and is due to a defect in AIRE ("autoimmune regulator"), a gene located on the 21st chromosome. Normal function of AIRE, a transcription factor, appears to be to confer immune tolerance for antigens from endocrine organs.



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