The Genetic Blueprint of PCD: Understanding How Primary Ciliary Dyskinesia Is Inherited
Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder that affects the microscopic, hair-like structures known as motile cilia. These tiny cellular structures act like biological motors and are found in the respiratory tract, reproductive system, and fluid-filled spaces of the brain.
When genetic mutations disrupt the instructions needed to build or control these structures, the cilia may be
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