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Accurate Test Results for FAT4 Gene Hennekam lymphangiectasia-lymphedema syndrome type 2 NGS Genetic DNA Test
FAT4 Gene Hennekam lymphangiectasia-lymphedema syndrome type 2 NGS Genetic DNA Test Cost 20000 Rs
FAT4 Gene Hennekam lymphangiectasia-lymphedema syndrome type 2 NGS Genetic DNA Test Details
FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis - DNA Labs India
Are you looking for information about FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 NGS Genetic DNA Test? Look no further than DNA Labs India. In this blog, we will discuss the cost, symptoms, and diagnosis of this genetic disorder.
What is FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2?
FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 is a rare genetic disorder that affects the lymphatic system. It is caused by mutations in the FAT4 gene, which provides instructions for making a protein that helps control the growth and division of cells. This disorder is characterized by swelling of the limbs, a buildup of lymphatic fluid, and abnormalities of the lymphatic vessels. It is also associated with intellectual disability and other developmental delays.
NGS Genetic DNA Test Cost
The cost of the NGS Genetic DNA Test for FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 is INR:20000 at DNA Labs India.
Symptoms of FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2
The symptoms of FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 can vary greatly from person to person. Some of the most common symptoms include:
- Swelling of the limbs
- A buildup of lymphatic fluid
- Abnormalities of the lymphatic vessels
- Intellectual disability
- Other developmental delays
Diagnosis of FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2
The diagnosis of FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 is typically made through genetic testing. This may involve a variety of different tests, including:
- NGS Genetic DNA Test
- Sanger Sequencing
- Deletion/Duplication Analysis
If you suspect that you or a loved one may be affected by FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2, it is important to speak with a genetic counselor or healthcare provider.
Conclusion
FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 is a rare genetic disorder that can have a significant impact on a person's quality of life. If you suspect that you or a loved one may be affected by this disorder, it is important to speak with a genetic counselor or healthcare provider. At DNA Labs India, we offer the NGS Genetic DNA Test for FAT4 Gene Hennekam Lymphangiectasia-Lymphedema Syndrome Type 2 at a cost of INR:20000. Contact us today to learn more.
Hennekam lymphangiectasia-lymphedema syndrome type 2 is a rare genetic disorder characterized by a combination of lymphangiectasia (abnormal dilation of lymphatic vessels) and lymphedema (swelling due to lymphatic system dysfunction). Mutations in the FAT4 gene have been associated with this condition.
The FAT4 gene provides instructions for producing a protein involved in cell adhesion and signaling processes. Mutations in the FAT4 gene can disrupt these processes, leading to the lymphatic abnormalities and lymphedema observed in Hennekam lymphangiectasia-lymphedema syndrome type 2.
An NGS (Next-Generation Sequencing) genetic DNA test for the FAT4 gene involves sequencing the DNA to identify any mutations or variations within the gene that could be linked to Hennekam lymphangiectasia-lymphedema syndrome type 2. This testing can help diagnose the condition and identify individuals who carry mutations in the FAT4 gene.
If you suspect that you or someone you know may have Hennekam lymphangiectasia-lymphedema syndrome type 2 or if there's a family history of the condition, it's important to consult with a healthcare professional, such as a geneticist or a lymphatic specialist. They can guide you through the genetic testing process, interpret the results, and provide appropriate recommendations for management and treatment based on the specific genetic findings.
