Osteogenesis Imperfecta tests in Dubai & UAE

Compare available Osteogenesis Imperfecta 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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Listed price range

2,800.00 AED

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Osteogenesis Imperfecta test prices

Showing 1–7 of 7 matching tests.

Osteogenesis Imperfecta diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4695 CRTAP Gene Osteogenesis Imperfecta Type VII Genetic Test This genetic test analyzes the CRTAP gene to identify mutations associated with Osteogenesis Imperfecta Type VII, a severe bone fragility disorder.	Peripheral Whole Blood or Buccal Swab / DNA Sample	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the CRTAP gene", "Copy number variants (deletions/duplications) in the CRTAP gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected diagnosis of Osteogenesis Imperfecta Type VII", "Genetic counseling for families with OI", "Prenatal diagnosis in at-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 93043-6 ICD-10: Q78.0, Z15.89, Z82.79 Clinical summary This genetic test analyzes the CRTAP gene to identify mutations associated with Osteogenesis Imperfecta Type VII, a severe bone fragility disorder.
TEST-4700 IFITM5 Gene Osteogenesis Imperfecta Type 5 Genetic Test This test identifies pathogenic variants in the IFITM5 gene, confirming a diagnosis of Osteogenesis Imperfecta type 5.	Whole blood, FTA card, or extracted genomic DNA	3–4 Weeks from sample receipt in laboratory	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the IFITM5 gene"] Parameters [] Preparation ["No special preparation such as fasting is required."] Indications ["Suspected Osteogenesis Imperfecta type 5", "Family history of Osteogenesis Imperfecta", "Need for definitive diagnosis for management planning"] Measurement technique Confirm with laboratory Codes LOINC: 21637-0 ICD-10: Q78.0 Clinical summary This test identifies pathogenic variants in the IFITM5 gene, confirming a diagnosis of Osteogenesis Imperfecta type 5.
TEST-4715 P3H1 Gene (Osteogenesis Imperfecta Type VIII) Genetic Test This test detects pathogenic variants in the P3H1 gene associated with autosomal recessive Osteogenesis Imperfecta Type VIII.	Peripheral Whole Blood (5 mL EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["P3H1 gene coding region", "P3H1 gene splice-site boundaries"] Parameters [] Preparation [] Indications ["Clinical suspicion of Osteogenesis Imperfecta Type VIII", "Unexplained recurrent fractures", "Family history of P3H1 mutations", "Carrier testing in consanguineous couples"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q78.0 Clinical summary This test detects pathogenic variants in the P3H1 gene associated with autosomal recessive Osteogenesis Imperfecta Type VIII.
TEST-4710 PLOD2 Gene Osteogenesis Imperfecta with Congenital Joint Contractures Genetic Test This genetic test analyzes the PLOD2 gene for pathogenic variants associated with Osteogenesis Imperfecta with Congenital Joint Contractures (Bruck syndrome type 2).	Peripheral whole blood (3–5 mL in EDTA tube) or FTA card for infants	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PLOD2 gene coding regions", "PLOD2 gene splice sites", "Pathogenic variants in PLOD2"] Parameters [] Preparation ["No fasting or special diet required", "Pre-test genetic counselling is mandatory", "Continue all current medications unless advised otherwise by physician"] Indications ["Suspected Osteogenesis Imperfecta with Congenital Joint Contractures (Bruck syndrome type 2)", "Patients with recurrent fractures, limb deformities, and fixed joint contractures"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q78.0 Clinical summary This genetic test analyzes the PLOD2 gene for pathogenic variants associated with Osteogenesis Imperfecta with Congenital Joint Contractures (Bruck syndrome type 2).
TEST-4690 PPIB Gene (Osteogenesis Imperfecta Type 9) Genetic Test This test evaluates the entire coding region of the PPIB gene for variants associated with Osteogenesis Imperfecta Type 9.	Peripheral whole blood, dried blood spot (FTA card), or extracted genomic DNA	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)", "Small insertions/deletions (indels)", "Copy-number changes"] Parameters [] Preparation [] Indications ["Suspected Osteogenesis Imperfecta Type 9", "Family history of Osteogenesis Imperfecta Type 9"] Measurement technique Confirm with laboratory Codes LOINC: 92819-6 ICD-10: Q78.0 Clinical summary This test evaluates the entire coding region of the PPIB gene for variants associated with Osteogenesis Imperfecta Type 9.
TEST-4718 SERPINF1 Gene Osteogenesis Imperfecta Type 6 Genetic Test This test analyzes the SERPINF1 gene for mutations associated with Osteogenesis Imperfecta type 6.	Peripheral blood (3–5 mL) or buccal swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SERPINF1 gene variants", "Copy Number Variants (CNVs) in SERPINF1"] Parameters [] Preparation ["Do not discontinue prescribed medication or calcium/vitamin D supplements without consulting your doctor."] Indications ["Suspected Osteogenesis Imperfecta type 6", "Family history of Osteogenesis Imperfecta"] Measurement technique Confirm with laboratory Codes LOINC: 76730-5 ICD-10: Q78.0 Clinical summary This test analyzes the SERPINF1 gene for mutations associated with Osteogenesis Imperfecta type 6.
TEST-4713 SERPINH1 Gene Osteogenesis Imperfecta Type 10 Genetic Test This genetic test analyzes the SERPINH1 gene to detect pathogenic variants associated with Osteogenesis Imperfecta Type 10.	Peripheral Whole Blood (3-5 mL in EDTA tube) or Buccal Swab	3–4 Weeks (Standard)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SERPINH1 gene sequence", "Pathogenic variants in SERPINH1"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected Osteogenesis Imperfecta Type 10", "Family history of Osteogenesis Imperfecta Type 10", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 82899-3 ICD-10: Q78.0 Clinical summary This genetic test analyzes the SERPINH1 gene to detect pathogenic variants associated with Osteogenesis Imperfecta Type 10.

Category overview

Osteogenesis Imperfecta: overview

Dealing with frequent, unexplained bone fractures in yourself or a child is incredibly distressing, but finding the exact biological cause brings empowering clarity and targeted relief. As a highly specialized offering in our Genetics department, testing for Osteogenesis Imperfecta focuses on mutations in the collagen genes responsible for bone strength and structure. By leveraging cutting-edge diagnostic technology, this precise molecular screening helps confirm this specific "brittle bone" condition, providing the definitive data needed to safely guide personalized orthopedic care and specialized pediatric oversight. Highly regarded for compassionate, specialized diagnostics among top diagnostic labs in the UAE, DNA Labs guarantees absolute patient confidentiality, unparalleled analytical precision, and prompt reporting. Protect your family's structural health—schedule your osteogenesis imperfecta testing in UAE, coordinate a convenient home sample collection, or connect with our medical genetics experts.

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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.