Pathology EMQ template.

Name: Stanford Wong

Theme: Lipoprotein Metabolism

 

OPTION LIST

 

A	Gain of function mutation of PCSK9	I	Loss of function mutation of PCSK9
B	CYP7A1 polymorphisms	J	Dominant mutation of truncated apoB
C	apoC II deficiency
D	apoA V deficiency
E	apoA-I mutations
F	Apo E2/2 genotype
G	MTP deficiency
H	ABC AI mutation

 

 

For each scenario below, choose the most appropriate answer from the list above. Each option may be used once, more than once or not at all.

 

1. Cause of Familial Primary Hypertriglyceridaemia type I

 

 

2. A rare cause of Familial Hypercholesterolaemia

 

 

3. Cause of Aβ-lipoproteinaemia

 

 

4. Cause of Hypoβ-lipoproteinaemia

 

 

5. Cause of Hypoα-lipoproteinaemia

 

 

 

ANSWERS

1.

2.

3.

4.

5.