Polyglandular autoimmune syndrome-type I.

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dc.contributor.authorJoshi, Rajesh Ren_US
dc.contributor.authorRao, Sudhaen_US
dc.contributor.authorPrabhu, S Sen_US
dc.date.accessioned2006-12-05en_US
dc.date.accessioned2009-05-27T06:00:31Z
dc.date.available2006-12-05en_US
dc.date.available2009-05-27T06:00:31Z
dc.date.issued2006-12-05en_US
dc.description.abstractPolyglandular 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.en_US
dc.description.affiliationDepartment of Pediatrics, B.J.Wadia Hospital for Children, Parel, Mumbai 400 012. rrj23@rediffmail.comen_US
dc.identifier.citationJoshi RR, Rao S, Prabhu SS. Polyglandular autoimmune syndrome-type I. Indian Pediatrics. 2006 Dec; 43(12): 1085-7en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/14419
dc.language.isoengen_US
dc.source.urihttps://indianpediatrics.neten_US
dc.subject.meshCandidiasis, Chronic Mucocutaneous --etiologyen_US
dc.subject.meshChilden_US
dc.subject.meshEctodermal Dysplasia --etiologyen_US
dc.subject.meshHumansen_US
dc.subject.meshHypoparathyroidism --etiologyen_US
dc.subject.meshMaleen_US
dc.subject.meshPolyendocrinopathies, Autoimmune --diagnosisen_US
dc.subject.meshPrognosisen_US
dc.titlePolyglandular autoimmune syndrome-type I.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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