Autoimmune polyglandular syndrome. Clinical experience in 21 cases

dc.creatorDevoto, Enzo
dc.creatorAravena C., Lucia
dc.creatorCorvalán M., Luis
dc.creatorLioi C., Ximena
dc.creatorMunizaga, Fernando
dc.creatorSoto I., Nestor
dc.creatorHidalgo V., M. Soledad
dc.creatorBarrera R., Radek
dc.creatorGajardo L., Hector
dc.date.accessioned2019-01-29T13:56:05Z
dc.date.available2019-01-29T13:56:05Z
dc.date.created2019-01-29T13:56:05Z
dc.date.issued1990
dc.identifierRevista medica de Chile, Volumen 118, Issue 6, 1990, Pages 635-642
dc.identifier00349887
dc.identifierhttps://repositorio.uchile.cl/handle/2250/160052
dc.description.abstractThe autoimmune polyglandular syndrome is characterized by the association of 2 or more endocrine disorders of autoimmune origin which may coexist with autoimmune disorders in other organs. Roughly 25% of patients with an autoimmune endocrinopathy show evidence of autoimmune disease elsewhere. We report 21 patients with autoimmune polyglandular syndrome classified according to Neufeld.
dc.languageen
dc.sourceRevista medica de Chile
dc.subjectMedicine (all)
dc.titleAutoimmune polyglandular syndrome. Clinical experience in 21 cases
dc.typeArtículo de revista


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