Authors: Mary A. Williamson Mt(ascp) Phd,L. Michael Snyder Md
Congenital deficiency of AAT
Tangier disease
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Alpha-2 globulin
Hereditary deficiency of Hp phenotypes
Nutritional deficiency, hepatocellular insufficiency, protein loss, intravascular hemolysis (decreased Hp)
Pancreatitis
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Betaglobulin
Chronic liver or renal disease
Hypobetalipoproteinemias
Thermal injuries
Acute inflammation
IgA deficiency
C3 degrades and eventually disappears in aged samples
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Gammaglobulin