DKC1 Gene Dyskeratosis congenita X-linked Genetic Test
Components: DKC1 Gene Dyskeratosis congenita X-linked Genetic Test
Price: 3200.0 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 DKC1 Gene Dyskeratosis congenita, X-linked NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DKC1 Gene Dyskeratosis congenita, X-linked NGS Genetic DNA Test gene DKC1
Test Details:
The DKC1 gene is associated with a rare genetic disorder called dyskeratosis congenita (DC), which primarily affects the skin, nails, and mucous membranes. It is an X-linked disorder, meaning it is typically inherited from the mother and primarily affects males. However, females can also be carriers of the mutated gene and may exhibit milder symptoms.
Next-generation sequencing (NGS) is a type of genetic test that can be used to analyze multiple genes simultaneously. In the case of DKC1 gene testing, NGS can be employed to identify mutations or variants in the DKC1 gene that may be responsible for dyskeratosis congenita.
NGS genetic testing for DKC1 gene mutations can help in the diagnosis of dyskeratosis congenita and provide valuable information about the risk of passing on the condition to future generations. It can also aid in genetic counseling and guide treatment options for affected individuals.
It is important to note that NGS testing is typically performed by a specialized laboratory or genetic testing facility. A healthcare professional, such as a geneticist or genetic counselor, can help determine if NGS testing for the DKC1 gene is appropriate in a given situation and guide individuals through the testing process.
Test Name | DKC1 Gene Dyskeratosis congenita X-linked Genetic Test |
---|---|
Components | |
Price | 3200.0 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 DKC1 Gene Dyskeratosis congenita, X-linked NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DKC1 Gene Dyskeratosis congenita, X-linked NGS Genetic DNA Test gene DKC1 |
Test Details |
The DKC1 gene is associated with a rare genetic disorder called dyskeratosis congenita (DC), which primarily affects the skin, nails, and mucous membranes. It is an X-linked disorder, meaning it is typically inherited from the mother and primarily affects males. However, females can also be carriers of the mutated gene and may exhibit milder symptoms. Next-generation sequencing (NGS) is a type of genetic test that can be used to analyze multiple genes simultaneously. In the case of DKC1 gene testing, NGS can be employed to identify mutations or variants in the DKC1 gene that may be responsible for dyskeratosis congenita. NGS genetic testing for DKC1 gene mutations can help in the diagnosis of dyskeratosis congenita and provide valuable information about the risk of passing on the condition to future generations. It can also aid in genetic counseling and guide treatment options for affected individuals. It is important to note that NGS testing is typically performed by a specialized laboratory or genetic testing facility. A healthcare professional, such as a geneticist or genetic counselor, can help determine if NGS testing for the DKC1 gene is appropriate in a given situation and guide individuals through the testing process. |