Skeletal Dysplasia tests in Dubai & UAE

Compare available Skeletal Dysplasia 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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Skeletal Dysplasia test prices

Showing 1–3 of 3 matching tests.

Skeletal Dysplasia diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4620 CTSK Gene Pycnodysostosis Genetic Test This genetic test evaluates the CTSK gene for mutations associated with pycnodysostosis, a rare bone disorder.	Whole Blood (2–5 mL EDTA), Extracted DNA, or Dried Blood Spot	14–21 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CTSK gene"] Parameters [] Preparation ["Discuss blood draw procedure with doctor if taking anticoagulants or antiplatelet drugs"] Indications ["Clinical history suggestive of pycnodysostosis", "Diagnosis of a rare osteochondrodysplasia"] Measurement technique Confirm with laboratory Codes LOINC: 95126-9 ICD-10: Q78.0 Clinical summary This genetic test evaluates the CTSK gene for mutations associated with pycnodysostosis, a rare bone disorder.
TEST-4531 DDR2 Gene Spondylometaepiphyseal Dysplasia (Short Limb‑Hand Type) Genetic Test This genetic test evaluates the DDR2 gene for mutations associated with Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type (SMD-SLH).	Whole Blood, Extracted DNA, or FTA Card (Peripheral Blood)	3–4 Weeks (expedited options available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DDR2 gene coding sequence variants", "Mutations associated with SMD-SLH"] Parameters [] Preparation ["Pre-test genetic counselling required", "Detailed pedigree chart mandatory"] Indications ["Clinical suspicion of Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type (SMD-SLH)", "Family history of SMD-SLH", "Need for genetic confirmation for diagnosis and management"] Measurement technique Confirm with laboratory Codes LOINC: 92730-6 ICD-10: Q77.8 Clinical summary This genetic test evaluates the DDR2 gene for mutations associated with Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type (SMD-SLH).
TEST-4534 MATN3 Gene Spondyloepimetaphyseal Dysplasia Genetic Test This genetic test identifies pathogenic variants in the MATN3 gene, confirming the genetic basis for spondyloepimetaphyseal dysplasia.	Peripheral 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 ["Pathogenic variants in the MATN3 gene", "Copy Number Analysis"] Parameters [] Preparation [] Indications ["Clinical suspicion of spondyloepimetaphyseal dysplasia", "Family history of skeletal dysplasia", "Need for definitive genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 94222-7 ICD-10: Q77.7 Clinical summary This genetic test identifies pathogenic variants in the MATN3 gene, confirming the genetic basis for spondyloepimetaphyseal dysplasia.

Category overview

Skeletal Dysplasia: overview

Concerns regarding a child’s disproportionate growth, short stature, or bone development demand compassionate, highly precise insights to establish a strong foundation of care. As a specialized offering in our Molecular Genetics services, Skeletal Dysplasia testing maps the specific genetic mutations responsible for abnormal cartilage and bone formation. Utilizing advanced diagnostic technology, this crucial molecular screening helps confirm exact developmental conditions, providing the definitive data needed to safely guide specialized pediatric orthopedics, physical therapy, and customized medical oversight. Trusted by parents across the top diagnostic labs in the UAE, DNA Labs is committed to strict patient confidentiality, unparalleled diagnostic accuracy, and highly efficient reporting. Protect your child's developmental trajectory—schedule your skeletal dysplasia testing in UAE, arrange a secure home sample collection, or connect with our specialized genetic counselors.

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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.