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FISH for William syndrome
SKU: MD-NLB391 Categories: , , , , , , , , , Tags: , , , , , , ,

In Stock

FISH for William syndrome

฿9,600.00

Additional information

Also Known As

Williams Syndrome FISH Test, Chromosomal Microdeletion (FISH), WS FISH
Specimen

Heparinized whole blood 5 ml. (Minimun Vol 3 ml.)
Turnaround Time

11 days
Test Code

MD-NLB391
Test Type

General
Related Tests

Chromosomal Microarray, Karyotyping

A fluorescence in situ hybridization (FISH) test that detects deletions in the 7q11.23 region of chromosome 7, associated with Williams syndrome. Used for early diagnosis, which is crucial for managing the cardiovascular and developmental issues.

Product tags: Chromosomal Microdeletion (FISH), Developmental Delays, Genetic Disorders, Heart Defects, None, William Syndrome, Williams Syndrome FISH Test, WS FISH
Diseases: Genetic Disorders, William Syndrome
Symptoms: Developmental Delays, Heart Defects
Habits: None
Age Groups: Children
Specimens: Blood
Diagnostic Methods: FISH, Genetic Testing
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Description

A fluorescence in situ hybridization (FISH) test that detects deletions in the 7q11.23 region of chromosome 7, associated with Williams syndrome. Used for early diagnosis, which is crucial for managing the cardiovascular and developmental issues.

This lab test includes home sample collection via a provided kit or by a clinician, and you'll receive a comprehensive physical health report with your results.

Additional information

Also Known As

Williams Syndrome FISH Test, Chromosomal Microdeletion (FISH), WS FISH
Specimen

Heparinized whole blood 5 ml. (Minimun Vol 3 ml.)
Turnaround Time

11 days
Test Code

MD-NLB391
Test Type

General
Related Tests

Chromosomal Microarray, Karyotyping

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