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Candidiasis and endocrinopathy syndrome

Authoring team

This is an autosomal recessive polyglandular deficiency state characterised by childhood onset and defective cellular immunity to Candida albicans which is refractory to conventional chemotherapy; however remission is reported with ketoconazole plus transfer factor. There is no HLA linkage.

The autoimmune element comprises:

  • hypoparathyroidism is common
  • diabetes is rare
  • adrenal insufficiency may develop acutely
  • pernicious anaemia
  • chronic active hepatitis
  • membranoproliferative glomerulonephritis
  • sprue

The associated disorders must be managed conventionally even if the Candida is successfully treated.


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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