Short Description

NGS genetic DNA test detecets for variant and mutation detection in ANTXR1 gene for Hemangioma capillary infantile

PreTest Information

Clinical History of Patient who is going for ANTXR1 Gene Hemangioma capillary infantile NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with ANTXR1 Gene Hemangioma capillary infantile NGS Genetic DNA Test gene ANTXR1

Detail Description

Understanding ANTXR1 Gene and Hemangioma Capillary Infantile

Hemangioma capillary infantile is a type of benign tumor that appears as a bright red or purplish spot on a baby's skin. It is usually harmless and tends to disappear on its own within a few years. However, in some cases, hemangioma capillary infantile can cause complications and require medical intervention.

The ANTXR1 gene has been linked to the development of hemangioma capillary infantile. This gene provides instructions for making a protein that is involved in the formation of blood vessels. When this gene is mutated or altered, it can cause abnormal blood vessel growth and lead to the development of hemangioma capillary infantile.

Symptoms of Hemangioma Capillary Infantile

The symptoms of hemangioma capillary infantile can vary depending on the location and size of the tumor. Some common symptoms include:

• A bright red or purplish spot on the skin
• A raised bump or lump
• Rapid growth of the tumor
• Pain or discomfort
• Ulceration or bleeding

Diagnosis of Hemangioma Capillary Infantile

Hemangioma capillary infantile is usually diagnosed through a physical examination of the affected area. In some cases, imaging tests such as ultrasound or MRI may be used to determine the extent of the tumor and its location.

Genetic testing can also be used to diagnose hemangioma capillary infantile. NGS (Next Generation Sequencing) genetic DNA test is a highly advanced and accurate testing method that can analyze multiple genes simultaneously and identify any mutations or alterations in the ANTXR1 gene that may be causing the tumor.

The Cost of NGS Genetic DNA Test for Hemangioma Capillary Infantile

The cost of NGS genetic DNA test for hemangioma capillary infantile can vary depending on the testing facility and the location. In India, the cost of this test is usually around INR 20,000.

While the cost of genetic testing may seem high, it is important to consider the potential benefits of early diagnosis. Genetic testing can help identify the underlying cause of hemangioma capillary infantile and allow for early intervention and treatment. This can prevent complications and improve the overall outcome for the affected child.

Conclusion

Genetic testing can play a crucial role in the diagnosis and management of hemangioma capillary infantile. By identifying any mutations or alterations in the ANTXR1 gene, healthcare providers can provide personalized treatment plans and improve the outcome for the affected child. While the cost of genetic testing may be a concern for some, it is important to consider the potential benefits and long-term savings in healthcare costs.

At DNA Labs India, we offer highly accurate and affordable NGS genetic DNA testing for hemangioma capillary infantile. Contact us today to learn more about our services and how we can help.

The ANTXR1 gene, also known as Anthrax Toxin Receptor 1 gene, is associated with various functions, including its role in facilitating the entry of anthrax toxins into cells. However, in the context of your question, it appears you are referring to a potential link between the ANTXR1 gene and hemangioma capillary infantile.

Hemangioma capillary infantile, also known as infantile hemangioma, is a common type of vascular birthmark that occurs in infants. It's characterized by the growth of benign blood vessels in the skin. While genetic factors may play a role in the development of hemangiomas, the precise genetic basis and the involvement of specific genes like ANTXR1 are not fully understood.

NGS (Next-Generation Sequencing) genetic DNA tests are a type of advanced genetic testing that can analyze multiple genes simultaneously. They are often used to identify genetic variations or mutations that may be associated with certain medical conditions or traits.