Polyglandular autoimmune syndrome-type I.
Indian Pediatr
;
2006 Dec; 43(12): 1085-7
Article
in English
| IMSEAR
| ID: sea-14419
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Prognosis
/
Humans
/
Male
/
Candidiasis, Chronic Mucocutaneous
/
Ectodermal Dysplasia
/
Child
/
Polyendocrinopathies, Autoimmune
/
Hypoparathyroidism
Type of study:
Prognostic study
Language:
English
Journal:
Indian Pediatr
Year:
2006
Type:
Article
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