JAGN1 Gene Neutropenia Severe Congenital Type 6 Autosomal Recessive Genetic Test
Welcome to DNA Labs UAE, where we offer the JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test. This test is designed to identify mutations or variations in the JAGN1 gene that may be causing severe congenital neutropenia type 6 (SCN6).
Test Components
The JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test includes:
- NGS Technology
- Osteology Dermatology Immunology Disorders
Price
The cost of the JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test is 4400.0 AED.
Sample Condition
We accept the following sample conditions for this test:
- Blood
- Extracted DNA
- One drop Blood on FTA Card
Report Delivery
You can expect to receive your test report within 3 to 4 weeks.
Method
We use NGS (Next-Generation Sequencing) technology for this genetic test.
Test Type
The JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test falls under the category of Osteology Dermatology Immunology Disorders.
Doctor
This test is conducted by a Dermatologist.
Test Department
Our Genetics department handles the JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test.
Pre Test Information
Before undergoing the JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive genetic test, we recommend providing us with the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with JAGN1 Gene Neutropenia, severe congenital type 6, autosomal recessive NGS Genetic DNA Test gene JAGN1.
Test Details
The JAGN1 gene is associated with severe congenital neutropenia type 6 (SCN6), an inherited condition. Neutropenia refers to a decrease in the number of neutrophils, a type of white blood cell that helps fight off infections. Our NGS genetic testing allows for the analysis of multiple genes simultaneously. In the case of SCN6, NGS genetic testing can identify mutations or variations in the JAGN1 gene that may be causing the condition. By analyzing the JAGN1 gene, our NGS genetic testing provides information about the presence of mutations or variations responsible for the development of SCN6. This information is crucial for making a definitive diagnosis, understanding the inheritance pattern, and providing appropriate genetic counseling and management options for affected individuals and their families.
Test Name | JAGN1 Gene Neutropenia severe congenital type 6 autosomal recessive 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 JAGN1 Gene Neutropenia, severe congenital type 6, autosomal recessive NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with JAGN1 Gene Neutropenia, severe congenital type 6, autosomal recessive NGS Genetic DNA Test gene JAGN1 |
Test Details |
The JAGN1 gene is associated with a condition called severe congenital neutropenia type 6 (SCN6), which is inherited in an autosomal recessive manner. Neutropenia refers to a decrease in the number of neutrophils, a type of white blood cell that helps fight off infections. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the case of SCN6, NGS genetic testing can be used to identify mutations or variations in the JAGN1 gene that may be causing the condition. By analyzing the JAGN1 gene, NGS genetic testing can provide information about the presence of mutations or variations that may be responsible for the development of SCN6. This information can help in making a definitive diagnosis, understanding the inheritance pattern, and providing appropriate genetic counseling and management options for affected individuals and their families. |