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Functions | Credit Management/Risk Management | Receivables Risk Management | Define and Assign Payment Guarantee Schemas | Define Customer Determination Schema Here you can assign a four-character alphanumeric key with a short description This key must be allocated to the customer master record in the billing view of the customer master record as seen in Figure 10-19

Hyperglycemia due to tissue insensitivity to insulin Hormonal tumors (acromegaly, Cushing s syndrome, glucagonoma, pheochromocytoma) Pharmacologic agents (corticosteroids, sympathomimetic drugs, niacin) Liver disease (cirrhosis, hemochromatosis) Muscle disorders (myotonic dystrophy) Adipose tissue disorders (lipodystrophy, truncal obesity) Insulin receptor disorders (acanthosis nigricans syndromes, leprechaunism) Hyperglycemia due to reduced insulin secretion Hormonal tumors (somatostatinoma, pheochromocytoma) Pancreatic disorders (pancreatitis, hemosiderosis, hemochromatosis) Pharmacologic agents (thiazide diuretics, phenytoin, pentamidine)

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decreased insulin release is an additional factor in producing carbohydrate intolerance, and with excess somatostatin production it is the major factor A rare syndrome of extreme insulin resistance associated with acanthosis nigricans afflicts either young women with androgenic features as well as insulin receptor mutations or older people, mostly women, in whom a circulating immunoglobulin binds to insulin receptors and reduces their affinity to insulin Medications such as diuretics, phenytoin, niacin, and high-dose corticosteroids can produce hyperglycemia that is reversible once the drugs are discontinued or when diureticinduced hypokalemia is corrected Chronic pancreatitis or subtotal pancreatectomy reduces the number of functioning B cells and can result in a metabolic derangement very similar to that of genetic type 1 diabetes except that a concomitant reduction in pancreatic A cells may reduce glucagon secretion so that relatively lower doses of insulin replacement are needed Insulin-dependent diabetes is occasionally associated with Addison s disease and autoimmune thyroiditis (Schmidt s syndrome, or polyglandular failure syndrome) This occurs more commonly in women and represents an autoimmune disorder in which there are circulating antibodies to adrenocortical and thyroid tissue, thyroglobulin, and gastric parietal cells

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