| APS I | Autoimmune polyendocrine syndrome type I |
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| polyendocrine deficiency syndrome | <syndrome> Polyglandular deficiency syndrome, associated pathologic dysfunction of several endocrine glands, as in Schmidt's syndrome. (05 Mar 2000) |
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| polyendocrine syndrome | <syndrome> Autoimmune disorder (the antigen to which the response is mounted is in the B-cells of the pancreas) in which there is involvement of several organ systems. (18 Nov 1997) |
| polyendocrine deficiency syndromes |
Type I: A disease that begins at about age 12, characterized by hypoparathyroidism, primary adrenal insufficiency, and mucocutaneous candidiasis. Alopecia, pernicious anemia, malabsorption, and chronic h
Ãâó:
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| polyendocrine |
pertaining to or affecting several endocrine glands. Called also polyadenous.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| polyendocrine autoimmune d.’s |
polyglandular autoimmune syndromes.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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