Bardet-Biedl Syndrome tests in Dubai & UAE

Compare available Bardet-Biedl Syndrome tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

2,800.00 AED

Clinical preparation

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Bardet-Biedl Syndrome test prices

Showing 1–4 of 4 matching tests.

Bardet-Biedl Syndrome diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3894 BBS7 Gene Bardet-Biedl Syndrome Type 7 Genetic Test This genetic test analyzes the BBS7 gene for mutations associated with Bardet-Biedl Syndrome Type 7.	Whole Blood (Peripheral)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Insertions", "Deletions", "Copy number variations (CNVs) in the BBS7 gene"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Suspected Bardet-Biedl Syndrome Type 7", "Family history of BBS7", "Cascade family screening"] Measurement technique Confirm with laboratory Codes LOINC: 82319-9 ICD-10: Q87.8 Clinical summary This genetic test analyzes the BBS7 gene for mutations associated with Bardet-Biedl Syndrome Type 7.
TEST-3889 BBS9 Gene Bardet-Biedl Syndrome Type 9 Genetic Test This test detects pathogenic variants in the BBS9 gene associated with Bardet-Biedl syndrome type 9.	Peripheral whole blood, extracted DNA, or one drop blood on 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 BBS9 gene", "Full gene coverage including deep intronic regions and CNV detection"] Parameters [] Preparation [] Indications ["Clinical suspicion of Bardet-Biedl syndrome type 9", "Known familial pathogenic variant"] Measurement technique Confirm with laboratory Codes LOINC: 81247-8 ICD-10: Q87.8, Z15.89, Z13.7 Clinical summary This test detects pathogenic variants in the BBS9 gene associated with Bardet-Biedl syndrome type 9.
TEST-3943 MKKS Gene Bardet-Biedl Syndrome Type 6 Genetic Testing Test This test identifies pathogenic variants in the MKKS gene associated with Bardet-Biedl Syndrome type 6.	Peripheral Whole Blood (EDTA), Extracted DNA, or FTA Card 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 MKKS gene"] Parameters [] Preparation ["Complete clinical history required", "Mandatory pre-test genetic counselling required"] Indications ["Clinical suspicion of Bardet-Biedl Syndrome type 6", "Family history of Bardet-Biedl Syndrome type 6", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81247-7 ICD-10: Q87.8, Z14.8, Z13.71 Clinical summary This test identifies pathogenic variants in the MKKS gene associated with Bardet-Biedl Syndrome type 6.
TEST-3940 TTC8 Gene Bardet-Biedl Syndrome Type 8 Genetic Test This genetic test analyzes the TTC8 gene for mutations associated with Bardet-Biedl Syndrome type 8.	Whole Blood, Extracted DNA, or FTA Card (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 TTC8 gene"] Parameters [] Preparation [] Indications ["Confirmation of suspected Bardet-Biedl Syndrome type 8", "Genetic counseling for individuals with relevant symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.89 Clinical summary This genetic test analyzes the TTC8 gene for mutations associated with Bardet-Biedl Syndrome type 8.

Category overview

Bardet-Biedl Syndrome: overview

Confronting complex, overlapping symptoms such as early-onset vision loss, obesity, or developmental delays in a child demands highly specific diagnostic care to unlock the right specialized support. As an elite offering in our rare disease Genetics department, Bardet-Biedl Syndrome testing meticulously evaluates specific genes (like BBS1 or BBS10) known to disrupt normal cellular cilia function. By leveraging state-of-the-art diagnostic technology, this crucial molecular screening helps confirm this intricate inherited condition, providing the definitive data needed to safely guide personalized pediatric endocrinology, ophthalmological interventions, and tailored educational support. Widely respected for sensitive pediatric diagnostics among premier diagnostic labs in Dubai and the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and rapid, dependable turnaround times. Empower your child’s developmental journey—book your Bardet-Biedl syndrome testing in UAE, arrange a secure clinical sample collection, or reach out to our dedicated genetic counselors.

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Use the test details as a conversation starter

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.