D0034
DiGeorge Syndrome (22q deletion)
Test Details: DiGeorge Syndrome is most commonly diagnosed by Fluorescence in situ hybridization (FISH) analysis. It is a disorder caused by the deletion of a segment of q arm of chromosome 22. Del 22q11.2 syndrome has many possible signs and symptoms that can affect almost any part of the body.
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Category
Cytogenetics
Pre-test Information
Clinical history is mandatory.
Report Delivery
3 working days
Gender
All
Organ
Multi-Organ
DiGeorge Syndrome (22q deletion)
4800
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