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ZBTB24 Gene Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The ZBTB24 Gene Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 (ICF2) Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the ZBTB24 gene. These mutations are responsible for causing Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome Type 2 (ICF2), a rare and complex genetic disorder. ICF2 is characterized by a weakened immune system, abnormalities in the stability of certain regions of chromosomes (centromeric instability), and distinctive facial features.

This genetic test involves analyzing the patient’s DNA to detect any aberrations in the ZBTB24 gene, which plays a crucial role in the development and function of the immune system. Early and accurate diagnosis through this test can help in managing the symptoms, preventing potential complications, and providing targeted treatments for those affected by ICF2.

The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. By offering this test, DNA Labs UAE provides essential support for the diagnosis and understanding of ICF2, facilitating better healthcare outcomes for individuals and families affected by this genetic condition.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 Genetic Test

Components: ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 Genetic Test

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test type: Dysmorphology

Doctor: Pediatrics

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 NGS Genetic DNA Test gene ZBTB24

Test Details: The ZBTB24 gene is associated with a rare genetic disorder called Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 (ICF2). This syndrome is characterized by immune system dysfunction, chromosomal instability, and distinct facial features. NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing method that can analyze multiple genes simultaneously. In the context of ICF2, NGS genetic testing can be used to identify mutations or variations in the ZBTB24 gene that may be responsible for the syndrome. By analyzing the entire coding region of the ZBTB24 gene, NGS testing can provide a comprehensive assessment of genetic variants that may be associated with ICF2. This can help in confirming a diagnosis, predicting disease progression, and guiding appropriate management and treatment options for individuals with suspected or confirmed ICF2.

Test Name ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ZBTB24 Gene Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 NGS Genetic DNA Test gene ZBTB24
Test Details

The ZBTB24 gene is associated with a rare genetic disorder called Immunodeficiency-centromeric instability-facial anomalies syndrome type 2 (ICF2). This syndrome is characterized by immune system dysfunction, chromosomal instability, and distinct facial features.

NGS (Next-Generation Sequencing) genetic testing refers to a high-throughput DNA sequencing method that can analyze multiple genes simultaneously. In the context of ICF2, NGS genetic testing can be used to identify mutations or variations in the ZBTB24 gene that may be responsible for the syndrome.

By analyzing the entire coding region of the ZBTB24 gene, NGS testing can provide a comprehensive assessment of genetic variants that may be associated with ICF2. This can help in confirming a diagnosis, predicting disease progression, and guiding appropriate management and treatment options for individuals with suspected or confirmed ICF2.

SKU: TEST-4176 Category:

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