Polyglandular autoimmune syndrome-type I.

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Date
2006-12-05
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Abstract
Polyglandular autoimmune syndrome type I is a rare disorder characterized by mucocutaneous candidiasis (MC), hypoparathyroidism (HP) and adrenal insufficiency , requiring regular follow up as the components of the syndrome appear at different age groups. We report a six and half year boy having this syndrome and presenting with MC, HP and ectodermal dystrophy.
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Joshi RR, Rao S, Prabhu SS. Polyglandular autoimmune syndrome-type I. Indian Pediatrics. 2006 Dec; 43(12): 1085-7
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https://imsear.searo.who.int/handle/123456789/14419
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Indian Pediatrics