Short Description

NGS genetic DNA test detecets for variant and mutation detection in ERCC5 gene for Xeroderma pigmentosum, group G

PreTest Information

Clinical History of Patient who is going for ERCC5 Gene Xeroderma pigmentosum, group G NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ERCC5 Gene Xeroderma pigmentosum, group G NGS Genetic DNA Test gene ERCC5

Detail Description

ERCC5 Gene Xeroderma pigmentosum, group G NGS Genetic DNA Test cost INR:20000 symptoms diagnosis

Xeroderma pigmentosum (XP) is a rare genetic disorder that affects the skin and eyes. It is caused by mutations in genes that are involved in repairing damaged DNA. People with XP are extremely sensitive to sunlight and are at high risk for developing skin cancer.

ERCC5 Gene and Xeroderma pigmentosum, group G

The ERCC5 gene is one of the genes that is involved in repairing damaged DNA. Mutations in this gene can cause Xeroderma pigmentosum, group G (XP-G), which is a subtype of XP. XP-G is a rare form of the disease that is characterized by severe sun sensitivity and an increased risk of skin cancer.

NGS Genetic DNA Test cost INR:20000

The NGS Genetic DNA Test for ERCC5 Gene Xeroderma pigmentosum, group G is a genetic test that can identify mutations in the ERCC5 gene. This test is performed using next-generation sequencing technology, which allows for the analysis of multiple genes at once. The cost of this test is INR 20000.

Symptoms of Xeroderma pigmentosum, group G

The symptoms of Xeroderma pigmentosum, group G can vary from person to person, but typically include:

• Severe sun sensitivity
• Blistering and peeling of the skin after sun exposure
• Freckling and dark spots on the skin
• Eye problems, such as photophobia (sensitivity to light) and eye irritation
• Increased risk of skin cancer, including melanoma

Diagnosis of Xeroderma pigmentosum, group G

Xeroderma pigmentosum, group G is diagnosed through a combination of clinical evaluation, family history, and genetic testing. A dermatologist or genetic counselor can help determine if genetic testing is appropriate based on a person's symptoms and family history. If a mutation is identified in the ERCC5 gene, a diagnosis of XP-G can be confirmed.

Conclusion

Xeroderma pigmentosum, group G is a rare genetic disorder that can cause severe sun sensitivity and an increased risk of skin cancer. The ERCC5 gene is one of the genes that is involved in repairing damaged DNA, and mutations in this gene can cause XP-G. The NGS Genetic DNA Test for ERCC5 Gene Xeroderma pigmentosum, group G is a genetic test that can identify mutations in the ERCC5 gene, and the cost of this test is INR 20000. If you or a loved one is experiencing symptoms of XP-G, it is important to speak with a dermatologist or genetic counselor to determine if genetic testing is appropriate.