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CDKN2A Gene Melanoma Cutaneous Malignant Familial Genetic Test Cost

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

-21%

The CDKN2A Gene Melanoma Cutaneous Malignant Familial Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, aimed at detecting mutations in the CDKN2A gene, which are strongly associated with an increased risk of developing familial cutaneous malignant melanoma. This test is particularly relevant for individuals with a family history of melanoma, as it can provide crucial information regarding their genetic predisposition to this aggressive form of skin cancer. By identifying specific genetic mutations, the test enables healthcare professionals to recommend personalized preventive measures, surveillance, and, if necessary, early intervention strategies to manage the risk. The cost of this comprehensive genetic test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze and interpret the genetic data.

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CDKN2A Gene Melanoma Cutaneous Malignant Familial Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab specializing in DNA testing and analysis. In this blog, we will discuss the CDKN2A Gene Melanoma Cutaneous Malignant Familial Genetic Test, its components, cost, symptoms, diagnosis, and more.

Test Name: CDKN2A Gene Melanoma Cutaneous Malignant Familial Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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: Cancer

Doctor: Oncologist

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for CDKN2A Gene Melanoma, cutaneous malignant, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CDKN2A Gene Melanoma, cutaneous malignant, familial NGS Genetic DNA Test gene CDKN2A

Test Details

The CDKN2A gene is a tumor suppressor gene that plays a crucial role in regulating cell division and preventing the development of cancer. Mutations in the CDKN2A gene have been associated with an increased risk of developing cutaneous malignant melanoma, which is a type of skin cancer.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations or variations. In the context of melanoma, NGS genetic testing can identify mutations in the CDKN2A gene that may increase an individual’s susceptibility to developing familial (inherited) melanoma.

Familial melanoma refers to cases where there is a strong family history of melanoma, suggesting a hereditary component. NGS genetic testing can help identify individuals who may carry mutations in the CDKN2A gene, which can inform their risk assessment and guide appropriate screening and preventive measures.

It is important to note that genetic testing for melanoma is typically recommended for individuals with a strong family history of the disease or those who have been diagnosed with multiple primary melanomas. Genetic counseling is often recommended prior to and after genetic testing to help individuals understand the implications of the results and make informed decisions about their healthcare.

Test Name CDKN2A Gene Melanoma cutaneous malignant familial 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 Cancer
Doctor Oncologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CDKN2A Gene Melanoma, cutaneous malignant, familial NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CDKN2A Gene Melanoma, cutaneous malignant, familial NGS Genetic DNA Test gene CDKN2A
Test Details

The CDKN2A gene is a tumor suppressor gene that plays a crucial role in regulating cell division and preventing the development of cancer. Mutations in the CDKN2A gene have been associated with an increased risk of developing cutaneous malignant melanoma, which is a type of skin cancer.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously for mutations or variations. In the context of melanoma, NGS genetic testing can identify mutations in the CDKN2A gene that may increase an individual’s susceptibility to developing familial (inherited) melanoma.

Familial melanoma refers to cases where there is a strong family history of melanoma, suggesting a hereditary component. NGS genetic testing can help identify individuals who may carry mutations in the CDKN2A gene, which can inform their risk assessment and guide appropriate screening and preventive measures.

It is important to note that genetic testing for melanoma is typically recommended for individuals with a strong family history of the disease or those who have been diagnosed with multiple primary melanomas. Genetic counseling is often recommended prior to and after genetic testing to help individuals understand the implications of the results and make informed decisions about their healthcare.