**Core Concept**
Kartagener's syndrome is a rare genetic disorder characterized by the triad of primary ciliary dyskinesia (PCD), chronic sinusitis, and situs inversus. This syndrome results from mutations in genes encoding for dynein arms, which are essential for ciliary motility.

**Why the Correct Answer is Right**
The correct answer is related to the pathophysiology of Kartagener's syndrome, which involves defects in the dynein arms of cilia. Dynein arms are responsible for the motility of cilia, and their dysfunction leads to impaired ciliary function, chronic sinusitis, and respiratory tract infections. The situs inversus in Kartagener's syndrome is thought to result from the abnormal ciliary motility during embryonic development.

**Why Each Wrong Option is Incorrect**
**Option A:** This option is incorrect because it does not accurately describe the characteristic of Kartagener's syndrome.
**Option B:** This option is incorrect because it is not a specific characteristic of Kartagener's syndrome, although it is a common feature of primary ciliary dyskinesia.
**Option C:** This option is incorrect because it is not a specific characteristic of Kartagener's syndrome.

**Clinical Pearl / High-Yield Fact**
It is essential to note that Kartagener's syndrome is a rare condition, but it is often associated with other genetic disorders, such as the immotile cilia syndrome (MCS) and the respiratory ciliary dyskinesia (RCD).

**Correct Answer:** D. Situs inversus