Genetic deficiency of complement factor causes:
**Core Concept**
The complement system is a group of proteins that play a crucial role in the innate immune response, helping to clear pathogens from the body. A deficiency in any of the complement factors can lead to impaired immune function, making individuals more susceptible to infections.
**Why the Correct Answer is Right**
A deficiency in complement factor C5 is a known cause of paroxysmal nocturnal hemoglobinuria (PNH), a rare disease characterized by the destruction of red blood cells. This occurs because C5 is a critical component of the membrane attack complex (MAC), which forms pores in the membranes of target cells, leading to their lysis. Without functional C5, the MAC cannot form, and red blood cells are more resistant to destruction. Additionally, C5 is also involved in the generation of C5a, a potent chemoattractant that recruits neutrophils to sites of infection.
**Why Each Wrong Option is Incorrect**
**Option A:** Complement factor C1q deficiency is associated with an increased risk of systemic lupus erythematosus (SLE) and Sjögren's syndrome, but it is not directly linked to paroxysmal nocturnal hemoglobinuria (PNH).
**Option B:** Complement factor C4 deficiency can also increase the risk of SLE and other autoimmune diseases, but it is not the primary cause of PNH.
**Option C:** Complement factor C3 deficiency is a rare condition that can lead to impaired immune function and increased susceptibility to infections, but it is not specifically associated with PNH.
**Clinical Pearl / High-Yield Fact**
A deficiency in complement factor C5 is a key factor in the pathogenesis of paroxysmal nocturnal hemoglobinuria (PNH), making it a critical component to consider in the diagnosis and management of this rare disease.
**Correct Answer:** C.