The Dysostosis Gene Panel is a specialized genetic test that examines a set of genes associated with various forms of dysostosis syndromes. Dysostosis syndromes are rare genetic disorders characterized by abnormal skeletal development. This panel helps identify specific genetic mutations or variations that may be responsible for the condition, aiding in accurate diagnosis and potentially guiding treatment options.
Blood
Documents Required for Dysostosis Gene Panel
• Doctor’s Prescription
A doctor’s note recommending the WGS test is required.
An OPD card is also acceptable.
• Health and Family History (If available)
Details about your health conditions and any similar health issues in your family.
This helps us understand if the condition may be genetic or environmental.
• Old Medical Reports (If available)
You can share any past medical records such as:
MRI scans, ultrasound reports, blood tests, ECG, TMT, etc.
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