Hyperchylomicronemia (type I) in childhood has been associated ...

[SAVANNAHHOOPER23]

Hyperchylomicronemi a (type I) in childhood has been associated with which of the following?
 
  A) Deficiencies of apolipoprotein CII and lipoprotein lipase
  B) Deficiencies of lipoprotein lipase and apolipoprotein AI
  C) Deficiencies of apolipoprotein CII, lipoprotein lipase, and apolipoprotein AI
  D) Deficiencies of apolipoprotein CII, LCAT, and apolipoprotein A1
  E) Deficiency of LCAT only

Question 2

What is the presumed defect in most cases of familial type IIa hyperlipoproteinemi a?
 
  A) Deficiency of hydroxymethylglutar yl (HMG)-CoA reductase
  B) Deficiency of cholesterol esterase
  C) Deficiency of lipoprotein lipase
  D) Defective receptors for LDL
  E) Defective esterifying enzymes LCAT and ACAT

[kingfahad97]

Answer to Question 1

Ans: A

Answer to Question 2

Ans: D

[SAVANNAHHOOPER23]

Great answer, keep it coming

[raenoj]

Thanks for the timely response, appreciate it