You are here: Home > Test Menu and Test Search Instructions > P > Primary Ciliary Dyskinesia (PCD) Mutation Testing (DNAl1 and DNAH5 genes)

Primary Ciliary Dyskinesia (PCD) Mutation Testing (DNAl1 and DNAH5 genes)

by Mike Rogers — last modified February 08, 2010 09:20 PM


UNC Hospitals
McLendon Clinical Laboratories
101 Manning Drive
Chapel Hill, NC 27514
 Tube Type
yellow top ACD tubeORpurple top tube

 

Test ID PCDSQ
Test Number 1549
SMS Browse 
PCD SEQUENCING
CPT Codes 83890, 83892 x9, 83898 x9, 83904 x9
Laboratory Molecular Genetics
Tube Station 30
SpecimenRoutine:3 mL blood, yellow top tube (ACD) or lavender top (EDTA) tube; See Important Comments
 Micro:1 mL blood, yellow top tube (ACD) or lavender top (EDTA) tube
AvailabilityRoutine:Weekdays
No weekends or holidays
 STAT:N/A
   
Turnaround Time 2-4 weeks .
Reference Range No mutations detected
Comments

Sequencing of selected exons in DNAI1 (exons 1, 13, 16, 17) and DNAH5 (exons 34, 50, 63, 76, 77) 
All blood specimens must be accompanied with a requisition and PCD clinical history form(see below).
Please call Lab (966-4408) with questions. Test used for SMS ordering and phlebotomy collection purposes. Reporting of results is done via CoPath and WEBCIS Molecular Genetics folder.

Additional Information:

  •  Primary Ciliary Dyskinesia (PCD) Foundation Brochure pdf.file
  •  PCD Clinical History Form pdf.file
  •  Molecular Genetics Test Request Form pdf.file 
  •  Directions for Collecting and Mailing specimens for Molecular Testing pdf.file

 

 

disclaimer text

Primary Ciliary Dyskinesia(PCD) Mutation Testing(DNAI1 and DNAH5 genes)

Document Actions