Primary Ciliary Dyskinesia tests in Dubai & UAE

Compare available Primary Ciliary Dyskinesia tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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2,800.00 AED

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Primary Ciliary Dyskinesia test prices

Showing 1–14 of 14 matching tests.

Primary Ciliary Dyskinesia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5572 CCDC103 Gene Primary Ciliary Dyskinesia (PCD Type 17) Genetic Test This genetic test identifies pathogenic variants in the CCDC103 gene associated with primary ciliary dyskinesia type 17.	Whole blood (3–5 mL in EDTA tube), extracted DNA, or FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CCDC103 gene", "Ciliary function impairment"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected primary ciliary dyskinesia", "Family history of PCD", "Recurrent respiratory infections"] Measurement technique Confirm with laboratory Codes LOINC: 82163-6 ICD-10: Q89.9, J98.9 Clinical summary This genetic test identifies pathogenic variants in the CCDC103 gene associated with primary ciliary dyskinesia type 17.
TEST-5564 CCDC114 Gene Primary Ciliary Dyskinesia Genetic Test (NGS) This test identifies pathogenic variants in the CCDC114 gene associated with Primary Ciliary Dyskinesia type 20.	Whole Blood, Buccal Swab, or Dried Blood Spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CCDC114 gene"] Parameters [] Preparation ["Detailed clinical evaluation recommended", "Genetic counselling session advised"] Indications ["Clinical suspicion of Primary Ciliary Dyskinesia (PCD)", "Family history of PCD", "Situs inversus", "Recurrent sino-pulmonary infections", "Infertility evaluation"] Measurement technique Confirm with laboratory Codes LOINC: 94807-4 ICD-10: Q34.8 Clinical summary This test identifies pathogenic variants in the CCDC114 gene associated with Primary Ciliary Dyskinesia type 20.
TEST-5524 CCDC39 Gene — Primary Ciliary Dyskinesia Type 14 — Genetic Test This genetic test analyzes the CCDC39 gene to identify mutations causing Primary Ciliary Dyskinesia Type 14 (PCD14). It detects single nucleotide variants, small insertions/deletio...	Peripheral whole blood (EDTA) or dried blood spot on FTA card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CCDC39 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No special fasting required", "Do not stop any medications prior to collection"] Indications ["Clinical suspicion of Primary Ciliary Dyskinesia Type 14", "Family history of PCD14", "Carrier screening in relatives of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: Q34.8 Clinical summary This genetic test analyzes the CCDC39 gene to identify mutations causing Primary Ciliary Dyskinesia Type 14 (PCD14). It detects single nucleotide variants, small insertions/deletions, and copy number changes.
TEST-5497 CCDC65 Gene Primary Ciliary Dyskinesia Type 27 Genetic Test This test evaluates the CCDC65 gene for pathogenic variants associated with Primary Ciliary Dyskinesia Type 27.	Whole Blood, Extracted DNA, or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CCDC65 gene", "Ciliary motility defects (indirectly)"] Parameters [] Preparation ["No fasting required", "Ensure prior radiological and microbiological reports are available"] Indications ["Diagnosis of Primary Ciliary Dyskinesia Type 27", "Family planning for individuals with PCD", "Confirmation of molecular basis for suspected PCD"] Measurement technique Confirm with laboratory Codes LOINC: 94194-6 ICD-10: J98.4; Q34.8 Clinical summary This test evaluates the CCDC65 gene for pathogenic variants associated with Primary Ciliary Dyskinesia Type 27.
TEST-5493 CCNO Gene Primary Ciliary Dyskinesia Type 29 Genetic Test This test identifies mutations in the CCNO gene associated with primary ciliary dyskinesia type 29.	Peripheral Whole Blood (Venipuncture), Extracted DNA, or FTA Card Blood Spot	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CCNO gene mutations", "Point mutations", "Indels", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["Continue all prescribed respiratory medications", "No medication washout required"] Indications ["Suspected primary ciliary dyskinesia type 29", "Family history of primary ciliary dyskinesia", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 88507-1 ICD-10: J98.4 Clinical summary This test identifies mutations in the CCNO gene associated with primary ciliary dyskinesia type 29.
TEST-5583 DNAAF1 Gene Primary Ciliary Dyskinesia Type 13 Test This test identifies pathogenic variants in the DNAAF1 gene associated with Primary Ciliary Dyskinesia Type 13.	Peripheral whole blood or buccal swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAAF1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Primary Ciliary Dyskinesia", "Chronic respiratory infections", "Situs inversus", "Family history of PCD"] Measurement technique Confirm with laboratory Codes LOINC: 51945-1 ICD-10: Q34.8 Clinical summary This test identifies pathogenic variants in the DNAAF1 gene associated with Primary Ciliary Dyskinesia Type 13.
TEST-5533 DNAAF2 Gene Analysis for Primary Ciliary Dyskinesia Type 10 (NGS) Test This test identifies pathogenic variants within the DNAAF2 gene associated with primary ciliary dyskinesia type 10.	Peripheral whole blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAAF2 gene sequence", "Pathogenic variants in DNAAF2"] Parameters [] Preparation ["No specific fasting required", "Avoid strenuous activity before sample collection"] Indications ["Suspected primary ciliary dyskinesia type 10", "Family history of primary ciliary dyskinesia", "Recurrent respiratory infections", "Infertility evaluation"] Measurement technique Confirm with laboratory Codes LOINC: 101034-4 ICD-10: Q34.8 Clinical summary This test identifies pathogenic variants within the DNAAF2 gene associated with primary ciliary dyskinesia type 10.
TEST-5510 DNAAF3 Gene Primary Ciliary Dyskinesia Type 2 Genetic Test This genetic test identifies mutations in the DNAAF3 gene associated with primary ciliary dyskinesia type 2 (PCD2). It helps confirm the diagnosis in individuals suspected of havin...	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot on FTA card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAAF3 gene mutations", "Ciliary function impairment"] Parameters [] Preparation ["No fasting required.", "Do not discontinue prescribed medications without consulting your physician."] Indications ["Suspected primary ciliary dyskinesia (PCD)", "Chronic respiratory infections", "Situs inversus", "Family history of PCD"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q34.8 Clinical summary This genetic test identifies mutations in the DNAAF3 gene associated with primary ciliary dyskinesia type 2 (PCD2). It helps confirm the diagnosis in individuals suspected of having this rare respiratory disorder.
TEST-5515 DNAAF5 Gene Primary Ciliary Dyskinesia Type 18 Genetic Test This test identifies pathogenic variants in the DNAAF5 gene associated with primary ciliary dyskinesia type 18.	Whole Blood (EDTA or FTA card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAAF5 gene pathogenic variants", "Complete DNAAF5 coding region and intron-exon boundaries"] Parameters [] Preparation ["No fasting required", "No medication restrictions, but list chronic therapies with sample"] Indications ["Suspected primary ciliary dyskinesia type 18", "Family history of primary ciliary dyskinesia", "Recurrent sino-pulmonary infections", "Neonatal respiratory distress"] Measurement technique Confirm with laboratory Codes LOINC: 2163-8 ICD-10: Q34.8 Clinical summary This test identifies pathogenic variants in the DNAAF5 gene associated with primary ciliary dyskinesia type 18.
TEST-5545 DNAH5 Gene (Primary Ciliary Dyskinesia Type 3) Genetic Test This test identifies pathogenic variants in the DNAH5 gene, confirming a diagnosis of Primary Ciliary Dyskinesia Type 3.	Whole Blood (Peripheral Venous Blood)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in DNAH5 gene coding exons"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Suspected Primary Ciliary Dyskinesia (PCD)", "Family history of PCD", "Chronic sinopulmonary disease"] Measurement technique Confirm with laboratory Codes LOINC: 21821-6 ICD-10: J98.8, Q34.8 Clinical summary This test identifies pathogenic variants in the DNAH5 gene, confirming a diagnosis of Primary Ciliary Dyskinesia Type 3.
TEST-5589 DNAI1 Gene Primary Ciliary Dyskinesia Type 1 Genetic Test This test evaluates the DNAI1 gene for mutations associated with primary ciliary dyskinesia type 1.	Peripheral whole blood, extracted DNA, or dried blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DNAI1 gene sequence", "DNAI1 gene copy number variations"] Parameters [] Preparation ["No specific fasting required", "Continue prescribed medications unless advised otherwise"] Indications ["Suspected primary ciliary dyskinesia type 1", "Chronic respiratory symptoms unresponsive to standard treatment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q34.8 Clinical summary This test evaluates the DNAI1 gene for mutations associated with primary ciliary dyskinesia type 1.
TEST-5489 HYDIN Gene Primary Ciliary Dyskinesia Type 5 Genetic Test This test identifies pathogenic variants in the HYDIN gene associated with Primary Ciliary Dyskinesia type 5 (PCD).	Whole Blood (EDTA), Extracted DNA, or Dried Blood Spot (FTA Card)	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HYDIN gene sequence", "Copy Number Variants (CNVs) in HYDIN gene"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "Documented clinical history recommended"] Indications ["Suspected Primary Ciliary Dyskinesia type 5", "Family history of PCD", "Need for definitive genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: J98.09 Clinical summary This test identifies pathogenic variants in the HYDIN gene associated with Primary Ciliary Dyskinesia type 5 (PCD).
TEST-5568 LRRC6 Gene Primary Ciliary Dyskinesia Type 19 Genetic Test This test detects pathogenic variants in the LRRC6 gene associated with Primary Ciliary Dyskinesia type 19.	Whole blood (EDTA), extracted DNA (≥1 µg), or dried blood spot (DBS)	21–28 business days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the LRRC6 gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required", "No medication adjustment required"] Indications ["Suspected Primary Ciliary Dyskinesia", "Family history of PCD", "Carrier screening", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 95274-1 ICD-10: Q34.8 Clinical summary This test detects pathogenic variants in the LRRC6 gene associated with Primary Ciliary Dyskinesia type 19.
TEST-5539 NME8 Gene Primary Ciliary Dyskinesia Type 6 Genetic Test This genetic test evaluates the NME8 gene for pathogenic variants associated with Primary Ciliary Dyskinesia type 6.	Whole blood or DNA FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NME8 gene", "Single nucleotide variants", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist if on anticoagulant therapy"] Indications ["Suspected Primary Ciliary Dyskinesia type 6", "Recurrent respiratory infections", "Family history of PCD", "Genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: J98.4 Clinical summary This genetic test evaluates the NME8 gene for pathogenic variants associated with Primary Ciliary Dyskinesia type 6.

Category overview

Primary Ciliary Dyskinesia: overview

Enduring chronic, unexplained respiratory infections or persistent sinus issues from childhood can be exhausting, but finding the exact biological root offers a clear path to relief. As an advanced offering within our Genetics department, testing for Primary Ciliary Dyskinesia (PCD) evaluates specific gene mutations that impair the microscopic hair-like structures in your respiratory tract. By leveraging state-of-the-art diagnostic technology, this crucial molecular screening helps confirm this rare inherited disorder, providing the definitive data needed to safely guide highly personalized pulmonary therapies and specialized medical management. Trusted for complex respiratory diagnostics among the best diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, uncompromising diagnostic precision, and prompt reporting. Take control of your respiratory health—book your primary ciliary dyskinesia testing in UAE, coordinate a secure home sample collection, or reach out to our medical genetics team.

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The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.