D0011
Deletion 7q11.23 William's Syndrome Blood
Test Details: William’s syndrome is a rare genetic condition characterized by unique physical features, delays in cognitive development and potential cardiovascular problems. It is caused by deletion of a specific segment of the q arm of chromosome 7. Fluorescence in situ hybridization (FISH) is a sensitive method to detect smaller genomic changes associated with various microdeletions.
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Category
Cytogenetics
Pre-test Information
Clinical history is mandatory.
Report Delivery
3 working days
Gender
All
Organ
Multi-Organ
Deletion 7q11.23 William's Syndrome Blood
4100
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