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HAX1 Gene Neutropenia Severe Congenital Type 3 Genetic Test Cost

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

-21%

The HAX1 Gene Neutropenia Severe Congenital Type 3 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the HAX1 gene, which are linked to Severe Congenital Neutropenia Type 3 (SCN3). This condition is a rare genetic disorder characterized by a marked decrease in the number of neutrophils, a type of white blood cell crucial for fighting off infections. Individuals with SCN3 are at a higher risk of recurrent infections, which can be life-threatening if not diagnosed and managed properly.

The test involves collecting a DNA sample, typically through a blood draw, and analyzing the genetic material for specific mutations in the HAX1 gene that are known to cause the disorder. This genetic test is critical for early diagnosis, allowing for timely intervention and management strategies to reduce the risk of infections and improve the quality of life for affected individuals.

The cost of the HAX1 Gene Neutropenia Severe Congenital Type 3 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis necessary to accurately diagnose this condition, guiding families and healthcare providers in making informed decisions regarding the care and treatment of patients with SCN3.

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HAX1 Gene Neutropenia severe congenital 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: Hematology
  • Doctor: Hematologist
  • Test Department: Genetics

Pre Test Information:

Clinical History of Patient who is going for HAX1 Gene Neutropenia, severe congenital type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HAX1 Gene Neutropenia, severe congenital type 3 NGS Genetic DNA Test gene HAX1.

Test Details:

The HAX1 gene is responsible for producing a protein called HCLS1-associated protein X-1, which is involved in the regulation of the immune system. Mutations in the HAX1 gene can lead to a rare genetic disorder known as severe congenital neutropenia type 3. Severe congenital neutropenia type 3 is characterized by a severe decrease in the number of neutrophils, a type of white blood cell that plays a crucial role in fighting off infections.

Individuals with this condition are highly susceptible to recurrent and severe bacterial infections, particularly in the respiratory tract, skin, and mucous membranes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the HAX1 gene. This type of testing can identify specific mutations or variations in the HAX1 gene that are associated with severe congenital neutropenia type 3.

NGS genetic testing can help in confirming a diagnosis of severe congenital neutropenia type 3, especially in cases where the clinical presentation is not clear. It can also be used for carrier testing and prenatal testing in families with a known HAX1 gene mutation.

By identifying the specific genetic mutation causing severe congenital neutropenia type 3, NGS genetic testing can provide valuable information for genetic counseling, management, and treatment options for affected individuals and their families.

Test Name HAX1 Gene Neutropenia severe congenital 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 Hematology
Doctor Hematologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for HAX1 Gene Neutropenia, severe congenital type 3 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HAX1 Gene Neutropenia, severe congenital type 3 NGS Genetic DNA Test gene HAX1
Test Details

The HAX1 gene is responsible for producing a protein called HCLS1-associated protein X-1, which is involved in the regulation of the immune system. Mutations in the HAX1 gene can lead to a rare genetic disorder known as severe congenital neutropenia type 3.

Severe congenital neutropenia type 3 is characterized by a severe decrease in the number of neutrophils, a type of white blood cell that plays a crucial role in fighting off infections. Individuals with this condition are highly susceptible to recurrent and severe bacterial infections, particularly in the respiratory tract, skin, and mucous membranes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes, including the HAX1 gene. This type of testing can identify specific mutations or variations in the HAX1 gene that are associated with severe congenital neutropenia type 3.

NGS genetic testing can help in confirming a diagnosis of severe congenital neutropenia type 3, especially in cases where the clinical presentation is not clear. It can also be used for carrier testing and prenatal testing in families with a known HAX1 gene mutation.

By identifying the specific genetic mutation causing severe congenital neutropenia type 3, NGS genetic testing can provide valuable information for genetic counseling, management, and treatment options for affected individuals and their families.

SKU: TEST-3929 Category:

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