Pancytopenia and Myelofibrosis in Autoimmune Polyglandular Syndrome Type I
β Scribed by Braskett, M.; Garcia-Lloret, M.I.; Howenstine, S.; McCurdy, D.; McGhee, S.
- Book ID
- 119278074
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 49 KB
- Volume
- 119
- Category
- Article
- ISSN
- 1097-6825
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π SIMILAR VOLUMES
Autoimmune polyglandular syndrome is characterized by a failure of multiple endocrine organs and the presence of circulating organ-specific autoantibodies targeted against the failing organs. Here we describe a patient with autoimmune polyglandular syndrome type I with the endocrine manifestations o
## Abstract A previously fit and well 35βyearβold man presented to the acute medical take with a threeβweek history of general malaise; he complained of polyuria, polydipsia, weight loss, abdominal pain and vomiting. He was diagnosed with type 1 diabetes (capillary blood glucose 20.7mmol/L) but was