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Case Reports
. 1997 Jun;76(6):532-4.
doi: 10.1136/adc.76.6.532.

Severe malabsorption in autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy syndrome successfully treated with immunosuppression

S Padeh  1 , R Theodor, A Jonas, J H Passwell
Affiliations
Case Reports

Severe malabsorption in autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy syndrome successfully treated with immunosuppression

S Padeh et al. Arch Dis Child. 1997 Jun.

Abstract

A 15 year old boy with autoimmune polyendocrinopathy-candidosis-ectodermal dystrophy syndrome suffered recurrent episodes of severe intractable diarrhoea, steatorrhoea, and hypocalcaemia. The only treatment modality, which controlled the malabsorption syndrome, was immunosuppression with intravenous high dose methylprednisolone and oral methotrexate maintenance therapy.

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