Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis (1216 page)

   Congenital deficiency of AAT

   Tangier disease

   
Alpha-2 globulin

   Hereditary deficiency of Hp phenotypes

   Nutritional deficiency, hepatocellular insufficiency, protein loss, intravascular hemolysis (decreased Hp)

   Pancreatitis

   
Betaglobulin

   Chronic liver or renal disease

   Hypobetalipoproteinemias

   Thermal injuries

   Acute inflammation

   IgA deficiency

   C3 degrades and eventually disappears in aged samples

   
Gammaglobulin