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DKC1 Gene Dyskeratosis Congenita X-Linked Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The DKC1 gene dyskeratosis congenita X-linked genetic test is a specialized diagnostic tool used to identify mutations in the DKC1 gene, which are linked to the rare genetic disorder dyskeratosis congenita. This condition primarily affects skin, nails, and bone marrow, leading to a variety of clinical manifestations including abnormal skin pigmentation, nail dystrophy, and a predisposition to bone marrow failure and cancer. Since the disorder follows an X-linked pattern of inheritance, it predominantly affects males, though female carriers may exhibit some symptoms.

The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed to detect any mutations in the DKC1 gene. This genetic testing is crucial for early diagnosis, which can significantly influence management and treatment strategies for affected individuals and their families.

The cost of the DKC1 gene dyskeratosis congenita X-linked genetic test at DNA Labs UAE is set at 3200 AED. While the price may seem steep, the value of obtaining a precise diagnosis cannot be overstated, as it opens the door to tailored treatments and interventions, as well as genetic counseling for families. Early and accurate detection through this test can greatly improve the quality of life for individuals with dyskeratosis congenita and assist in the management of the condition’s various complications.

Description

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.