**Core Concept**
Wiskott-Aldrich Syndrome (WAS) is a rare, X-linked recessive disorder characterized by eczema, thrombocytopenia, and recurrent infections. It is caused by mutations in the WAS gene, leading to impaired function of the Wiskott-Aldrich Syndrome protein (WASP), which is crucial for platelet signaling, immune cell development, and function.

**Why the Correct Answer is Right**
The correct answer will be the statement that does not accurately describe the clinical manifestations or pathophysiology of WAS. The WAS protein plays a key role in the regulation of the actin cytoskeleton in platelets and immune cells, thereby affecting their function and survival. The syndrome is characterized by impaired platelet aggregation, increased susceptibility to infections, and eczema due to immune dysregulation.

**Why Each Wrong Option is Incorrect**
**Option A:** WAS is characterized by thrombocytopenia, but it is also associated with platelet dysfunction, which leads to impaired platelet aggregation and bleeding tendency.
**Option B:** WAS patients are indeed susceptible to recurrent infections, particularly those caused by opportunistic pathogens, due to impaired immune cell function.
**Option C:** WAS is not primarily associated with autoimmune disorders, although some patients may develop autoimmune complications due to immune dysregulation.

**Clinical Pearl / High-Yield Fact**
WAS is a classic example of an X-linked recessive disorder that predominantly affects males, as the WAS gene is located on the X chromosome. Carrier females may exhibit mild symptoms or be asymptomatic.

**Correct Answer:** C.