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Lahalak Medical PlatformDifferentiate Care
FISH for DiGeorge (22q11.2 Deletion) Syndrome
A precise genetic test to detect 22q11.2 chromosome deletion, aiding in the early diagnosis of DiGeorge syndrome and related disorders to ensure optimal medical care for your child.
An advanced laboratory test using FISH technology to detect the deletion of a small segment of chromosome 22, the primary cause of DiGeorge syndrome and associated cardiac or immune issues.
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