Primary Ciliary Dyskinesia (PCD) Mutation Testing

Tube type

Test ID		LAB5674
EPIC Order		PCD SEQUENCING
CPT Codes		81407, G0452
Laboratory		Molecular Genetics Laboratory
Tube Station		30
Specimen	Routine:	3 mL blood, yellow ACD-A tube or lavender EDTA tube; See Comments
	Micro:	1 mL blood, yellow ACD-A tube or lavender EDTA tube
Availability	Routine:	Weekdays; no weekends or holidays
Turnaround Time		14-28 days
Reference Range		No mutations detected
Comments	Sequencing the complete coding region and flanking regions of 35 genes associated with PCD. See link below for description. All blood specimens must be accompanied with a requisition and PCD clinical history form(see below). Please call Lab (984-974-1825) with questions. Additional Information: Primary Ciliary Dyskinesia (PCD) Foundation Brochure pdf.file PCD Clinical History Form pdf.file Primary Ciliary Dyskinesia/Kartagener Syndrome (PCD) pdf. file Molecular Genetics Test Request Form pdf.file Directions for Collecting and Mailing specimens for Molecular Testing pdf.file

Reviewed by J. Carr on November 20, 2025

UNC Hospitals
McLendon Clinical Laboratories
101 Manning Drive
Chapel Hill, NC 27514