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TYK2 Gene Tyrosine kinase 2 deficiency Genetic Test Cost

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

-21%

The TYK2 Gene Tyrosine kinase 2 deficiency genetic test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the TYK2 gene, which can lead to a rare immunodeficiency disorder. Tyrosine kinase 2 (TYK2) is an enzyme that plays a crucial role in the signaling pathways of various cytokines, influencing immune responses. Deficiencies or dysfunctions in this gene can lead to increased susceptibility to infections and potentially impact the patient’s immune system regulation.

The test is crucial for individuals who exhibit symptoms of immune deficiency, recurrent infections, or have a family history of similar issues, as it can provide a definitive diagnosis. This enables healthcare providers to tailor treatment strategies more effectively, potentially improving the patient’s quality of life.

At DNA Labs UAE, the test is conducted with the utmost precision and confidentiality. The cost of the TYK2 Gene Tyrosine kinase 2 deficiency genetic test is set at 4400 AED. This investment covers the comprehensive analysis required to detect any anomalies in the TYK2 gene, ensuring that patients receive accurate and actionable insights into their condition.

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TYK2 Gene Tyrosine kinase 2 deficiency Genetic Test

Test Name: TYK2 Gene Tyrosine kinase 2 deficiency Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for TYK2 Gene Tyrosine kinase 2 deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosine kinase 2 deficiency.

Test Details: The TYK2 gene is responsible for encoding the tyrosine kinase 2 protein, which plays a role in the immune system’s response to various signals. TYK2 deficiency refers to a genetic condition in which there is a mutation or alteration in the TYK2 gene, leading to reduced or impaired function of the TYK2 protein.

NGS (Next-Generation Sequencing) is a type of genetic test that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of TYK2 deficiency, NGS can be used to identify mutations or alterations in the TYK2 gene, helping to diagnose individuals with this condition.

By analyzing the genetic information obtained through NGS, healthcare professionals can identify specific mutations or alterations in the TYK2 gene that may be causing the deficiency. This information can be useful in understanding the underlying cause of the condition and may help guide treatment decisions or genetic counseling.

Test Name TYK2 Gene Tyrosine kinase 2 deficiency 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 Metabolic Disorders
Doctor General Physician
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TYK2 Gene Tyrosine kinase 2 deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Tyrosine kinase 2 deficiency
Test Details

The TYK2 gene is responsible for encoding the tyrosine kinase 2 protein, which plays a role in the immune system’s response to various signals. TYK2 deficiency refers to a genetic condition in which there is a mutation or alteration in the TYK2 gene, leading to reduced or impaired function of the TYK2 protein.

NGS (Next-Generation Sequencing) is a type of genetic test that allows for the simultaneous sequencing of multiple genes or even the entire genome. In the context of TYK2 deficiency, NGS can be used to identify mutations or alterations in the TYK2 gene, helping to diagnose individuals with this condition.

By analyzing the genetic information obtained through NGS, healthcare professionals can identify specific mutations or alterations in the TYK2 gene that may be causing the deficiency. This information can be useful in understanding the underlying cause of the condition and may help guide treatment decisions or genetic counseling.