Mon Jun 26 2017

Search Results: diabetes



Sudden-Onset Diabetes Mellitus

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Diabetes mellitus characterized by insulin deficiency, sudden onset, severe hyperglycemia, rapid progression to ketoacidosis, and death unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence



Streptozocin Diabetes

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Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by pancreatectomy



Streptozotocin Diabetes

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Diabetes mellitus induced experimentally by administration of various diabetogenic agents or by pancreatectomy



Stable Diabetes Mellitus

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Diabetes characterized by the ability to survive without ketoacidosis in the absence of insulin therapy. It is usually of slow onset and patients exhibit a tendency to obesity



Slow-Onset Diabetes Mellitus

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Diabetes characterized by the ability to survive without ketoacidosis in the absence of insulin therapy. It is usually of slow onset and patients exhibit a tendency to obesity



Renal Diabetes

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Glycosuria occurring when there is only the normal amount of sugar in the blood, due to inherited inability of the renal tubules to reabsorb glucose completely. (Dorland, 27th ed)



Pregnancy-Induced Diabetes

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Either symptomatic diabetes or impaired glucose tolerance induced by pregnancy but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS)



Pregnancy in Diabetes

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Previously diagnosed diabetics that become pregnant. This does not include either symptomatic diabetes or impaired glucose tolerance induced by pregnancy but resolved at the end of pregnancy (DIABETES, GESTATIONAL)



Pituitary Diabetes Insipidus

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Deficiency of vasopressin secretion from the posterior pituitary gland. Clinical manifestations include extreme thirst, polydipsia, and reduced serum osmolality. Potential etiologies include CRANIOCEREBRAL TRAUMA; post-neurosurgical states; HYPOTHALAMIC NEOPLASMS; PITUITARY NEOPLASMS; CENTRAL NERVOUS SYSTEM INFECTIONS; PITUITARY APOPLEXY; CEREBROVASCULAR DISORDERS; granulomatous diseases (including SARCOIDOSIS); and other conditions. The disorder may also be inherited as an autosomal or recessive trait. (From Joynt, Clinical Neurology, 1992, Ch 36, pp55-8)



Phosphate Diabetes

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Familial disorder characterized by hypophosphatemia associated with decreased renal tubular reabsorption of inorganic phosphorus. It is sometimes associated with osteomalacia or rickets which do not respond to the usual doses of vitamin








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