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HOXB1 Gene Facial paresis type 3 NGS Genetic DNA Test Cost 20000 Rs
HOXB1 Gene Facial paresis type 3 NGS Genetic DNA Test Details
HOXB1 Gene Facial Paresis Type 3 NGS Genetic DNA Test Cost INR:20000 Symptoms Diagnosis
Facial paresis, also known as facial paralysis, is a condition that affects the muscles of the face, making it difficult or impossible to make facial expressions. There are several different types of facial paresis, each caused by a different underlying condition. One type of facial paresis is caused by a genetic mutation in the HOXB1 gene. DNA Labs India offers a NGS genetic DNA test for this condition at a cost of INR 20,000. Here's what you need to know about facial paresis caused by the HOXB1 gene:
Symptoms of HOXB1 Gene Facial Paresis Type 3
The symptoms of HOXB1 gene facial paresis type 3 typically appear in early childhood. They may include:
- Weakness or paralysis on one or both sides of the face
- An inability to close one or both eyes
- A drooping or uneven smile
- Difficulty making facial expressions
These symptoms may be mild or severe, and they may affect one side of the face more than the other.
Diagnosis of HOXB1 Gene Facial Paresis Type 3
Diagnosing HOXB1 gene facial paresis type 3 typically involves a combination of physical examination, medical history, and genetic testing. Your doctor may perform a physical examination to assess the strength and movement of your facial muscles. They may also ask about your symptoms and medical history.
To confirm a diagnosis of HOXB1 gene facial paresis type 3, your doctor may recommend genetic testing. This may involve a blood test or a cheek swab to collect a sample of your DNA. The sample will be sent to a laboratory for analysis, and the results will typically be available within a few weeks.
NGS Genetic DNA Test for HOXB1 Gene Facial Paresis Type 3 Cost
The NGS genetic DNA test for HOXB1 gene facial paresis type 3 is available through DNA Labs India at a cost of INR 20,000. This test uses next-generation sequencing technology to analyze your DNA and look for mutations in the HOXB1 gene. The test is non-invasive and typically involves a simple blood draw or cheek swab.
If you are experiencing symptoms of facial paresis or have a family history of the condition, it may be worth considering genetic testing. Identifying the underlying cause of your symptoms can help your doctor develop an effective treatment plan and provide you with valuable information about your health.
Conclusion
Facial paresis caused by a mutation in the HOXB1 gene is a rare but potentially serious condition that can cause weakness or paralysis of the facial muscles. If you are experiencing symptoms of facial paresis or have a family history of the condition, it may be worth considering genetic testing. DNA Labs India offers a NGS genetic DNA test for HOXB1 gene facial paresis type 3 at a cost of INR 20,000. Talk to your doctor to learn more about whether this test may be right for you.
Before getting tested ask for Raw Data, FASTQ, and VCF files along with clinical test report from DNA Testing Lab. DNA Labs India is the Only lab that is transparent and will share Raw Data, FASTQ, and VCF files along with the conclusive clinical report for HOXB1 Gene Facial paresis type 3 NGS Genetic DNA Test