What is the mechanism unedrlying familial hypercholesterolaemia?
LDL Receptor mutation (Autosomal ddominant) whose severity depensd on receptor functionality
LDL cholesterol 9-10 mmol/L is suggestive of what?
Heterzygote form => moderate to severe
Management of Familial Hypercholesterolaemia?
1st line: High-dose Statin
2nd line:
3rd line: PCSK9 inhibitor: Evolocumab
What complement deficiencies are present in SLE?
C1q + C1rs + C2 + C4
C5 deficiency is associated with what condition?
Leiner’s disease present in infancy with darrhoea, seborrheic dermatitis
C3 and C5-9 deficiencies are associated with what?
Neisseiria meningitidis (meningococcal meningitis)
Most common non-atherotic angina cause?
Aortic regurgitation => imbalance between oxygen supply and demand
Other causes: thyrotoxicosis - AS - HCM - Anaemia
What’s the predominant acid-base abnormality in ureteric diversion?
Metabolic acidosis