Wallach's Interpretation of Diagnostic Tests: Pathways to Arriving at a Clinical Diagnosis (730 page)

Apo A-1 Increased In

   Familial hyperalphalipoproteinemia (a rare genetic disorder)

Apo A-1 Decreased In

   Nephrosis and chronic renal failure

   Familial hypoalphalipoproteinemia (rare genetic disorder)

   Uncontrolled diabetes

   Apo C-II deficiency

   Apo A-1 melano disease

   Apo A-1-C-III deficiency

   Hepatocellular disease

   Parkinson disease

Apo-B Disorders Increased In

   Hepatic disease

   Hyperlipoproteinemia IIa, IIb, and V

   Cushing syndrome

   Porphyria

   Werner syndrome