William’s Syndrome – Microdeletion of Chromosome 7q11.23
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The William’s Syndrome – Microdeletion of Chromosome 7q11.23 test is a genetic diagnostic test designed to detect deletions on the 7q11.23 region of chromosome 7, which are associated with William’s Syndrome. This test helps in early diagnosis, genetic counseling, and management planning for individuals suspected to have William’s Syndrome.
Test Method: Microdeletion analysis using techniques such as FISH (Fluorescence In Situ Hybridization) or Chromosomal Microarray.
Sample Type: Blood (Peripheral Blood Sample)
Turnaround Time: Typically 7–14 days
Key Benefits:
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✅ Early detection of William’s Syndrome in children and adults
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✅ Supports informed genetic counseling for families
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✅ Helps in planning personalized management and care
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✅ Provides clarity on suspected developmental or cardiac anomalies
Formula Highlights:
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Detects deletions specifically at the 7q11.23 locus
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High sensitivity and specificity for microdeletions
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Non-invasive sample collection
Usage Instructions:
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Blood sample to be collected by trained personnel
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Avoid hemolysis; ensure proper sample storage and transport
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Follow clinician’s instructions for pre-test consultation
Additional Information:
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Suitable for suspected developmental delays, cardiovascular anomalies, or distinctive facial features
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Recommended to be interpreted by a certified genetic counselor or physician
What You Receive:
Safety & Care:
Free From:
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