Digeorge Syndrome, 22Q11.2 Deletion, FISH

Available viaHome Collection
GenderMale & Female
Contains6 parameters
Earliest reports in6 Working Days
PreparationNo preparation needed

Overview of Digeorge Syndrome, 22Q11.2 Deletion, FISH in Kochi

What is the DiGeorge Syndrome 22q11.2 Deletion FISH test?

 This test detects deletions in chromosome 22q11.2, which are associated with DiGeorge syndrome, a genetic disorder affecting multiple organ systems.


Why is this test performed?

 It is used to diagnose DiGeorge syndrome in individuals with congenital heart defects, immune deficiencies, and developmental delays.


How is the test conducted?

 A blood sample is analyzed using fluorescence in situ hybridization (FISH) to detect chromosome deletions.


What do abnormal results indicate?

 A confirmed deletion in 22q11.2 suggests DiGeorge syndrome, which may require lifelong medical management.


What are the next steps if the test is positive?

 Treatment plans may include cardiac care, immune system monitoring, and early developmental interventions.

Test included

Digeorge Syndrome, 22Q11.2 Deletion, FISH includes 6 parameters

  • Specimen
  • Clinical Indications
  • Total Number Of Cells
  • Digeorge Syndrome, 22q11.2 Deletion , Fish
  • Normal
  • Interpretation

Test code

6022F

CPT and Loinc codes

Department

  • Cytogenetics

Turn around time

6 Working Days

Test run frequency

Every Day TIME - 07:00

Performing locations

1 labs across India

Specimen vol. and vacutainer information

SpecimenVacutainerVolume
Heparin Whole BloodGreen Vacutainer2 ML

Specimen stability information

Heparin Whole Blood

Digeorge Syndrome, 22Q11.2 Deletion, FISH

₹6950

Health Checkup Category

Complete Care Packages

DIGEORGE SYNDROME, 22Q11.2 DELETION , FISH Test in Other Cities

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