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

BOOK: Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis
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   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

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