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UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 Genetic Test

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

-21%

The UNC13D gene plays a critical role in the immune system, specifically in the function of natural killer (NK) cells and cytotoxic T lymphocytes. Mutations in the UNC13D gene are associated with a severe and potentially fatal immune disorder known as Hemophagocytic Lymphohistiocytosis type 3 (HLH-3). This genetic condition is characterized by an overactive, poorly regulated immune response that leads to widespread inflammation and tissue damage.

To diagnose this condition, a genetic test targeting the UNC13D gene can be conducted. This test is crucial for individuals suspected of having HLH-3, as early diagnosis and treatment are vital for improving outcomes. The test involves analyzing the patient’s DNA to identify mutations in the UNC13D gene that are known to cause the disorder.

In the UAE, DNA Labs offers this specialized genetic test for Hemophagocytic Lymphohistiocytosis type 3. The cost of the test is 4400 AED. Conducting this test at DNA Labs UAE provides patients and healthcare providers with critical information for the management of HLH-3, including decisions about treatment strategies and potential genetic counseling for affected families.

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UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test gene UNC13D.

Test Details:

The UNC13D gene is associated with a condition called hemophagocytic lymphohistiocytosis type 3 (HLH-3). HLH is a rare and life-threatening immune disorder characterized by an overactivation of the immune system. It can result in excessive inflammation and damage to various organs in the body.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of HLH-3, NGS genetic testing can be used to identify mutations or variations in the UNC13D gene that may be associated with the condition. This type of testing can help with the diagnosis of HLH-3 and may also be used for genetic counseling and family planning purposes.

It’s important to note that genetic testing for HLH-3 is typically performed in specialized laboratories and is ordered by a healthcare professional. The results of the genetic test, along with other clinical and laboratory findings, can help guide treatment decisions and management of the condition.

Test Name UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UNC13D Gene Hemophagocytic lymphohistiocytosis type 3 NGS Genetic DNA Test gene UNC13D
Test Details

The UNC13D gene is associated with a condition called hemophagocytic lymphohistiocytosis type 3 (HLH-3). HLH is a rare and life-threatening immune disorder characterized by an overactivation of the immune system. It can result in excessive inflammation and damage to various organs in the body.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously. In the context of HLH-3, NGS genetic testing can be used to identify mutations or variations in the UNC13D gene that may be associated with the condition. This type of testing can help with the diagnosis of HLH-3 and may also be used for genetic counseling and family planning purposes.

It’s important to note that genetic testing for HLH-3 is typically performed in specialized laboratories and is ordered by a healthcare professional. The results of the genetic test, along with other clinical and laboratory findings, can help guide treatment decisions and management of the condition.