Serum C3 is persistently low in the following except –
Common causes of low C3 include post-streptococcal glomerulonephritis, where the alternative pathway is activated. Also, in systemic lupus erythematosus (SLE), the classical pathway is often involved, leading to C3 consumption. Membranoproliferative glomerulonephritis (MPGN) is another condition where C3 levels are low because the alternative pathway is active. Then there's C3 deficiency itself, which is a primary immunodeficiency.
Now, the question is asking for the exception. So, which condition does NOT cause persistent low C3? Let's think. For example, in hereditary angioedema, the issue is with C1 inhibitor, not directly affecting C3. Or maybe in some cases of acute glomerulonephritis, C3 might be low temporarily but not persistently. Wait, post-streptococcal is usually acute, and C3 recovers. But MPGN is chronic, so C3 remains low. SLE is chronic. So maybe the answer is post-streptococcal glomerulonephritis because it's acute and C3 levels recover after a few weeks. So the exception is post-streptococcal GN.
Now, I need to structure the explanation. The core concept is about complement system and C3 consumption. The correct answer is post-streptococcal GN because it's acute and C3 normalizes. The wrong options are SLE, MPGN, and C3 deficiency. Hereditary angioedema is another distractor but maybe not in the options. Wait, the options are A to D, but the user didn't list them. Hmm, but the correct answer is given as, say, A. So I need to make sure the options are correct. Let me check again.
The correct answer is the one where C3 isn't persistently low. Post-streptococcal GN is acute, C3 drops initially but recovers. So the exception is that condition. The other conditions (SLE, MPGN, C3 deficiency) have persistent low C3. So the correct answer is post-streptococcal GN. The clinical pearl is that persistent low C3 points to chronic conditions like MPGN or SLE, while acute cases like post-strep recover. That should be the high-yield fact.
**Core Concept**
Serum C3 levels are persistently low in conditions involving chronic activation of the complement system, such as systemic lupus erythematosus (SLE), membranoproliferative glomerulonephritis (MPGN), or C3 deficiency. Transient C3 depletion occurs in acute post-infectious conditions like post-streptococcal glomerulonephritis (PSGN), where levels normalize after recovery.
**Why the Correct Answer is Right**
**Post-streptococcal glomerulonephritis