Short Description

NGS genetic DNA test detecets for variant and mutation detection in RBM10 gene for Tarp syndrome

PreTest Information

Clinical History of Patient who is going for RBM10 Gene Tarp syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with RBM10 Gene Tarp syndrome NGS Genetic DNA Test gene RBM10

Detail Description

RBM10 Gene and Tarp Syndrome: Understanding the Symptoms, Diagnosis, and NGS Genetic DNA Test Cost in India

Recent advancements in genetic research have led to the identification of various genes responsible for causing specific medical conditions. One such gene is the RBM10 gene, which is associated with Tarp syndrome. Tarp syndrome is a rare genetic disorder that affects multiple organs and systems of the body.

What is Tarp Syndrome?

Tarp syndrome is a rare genetic disorder that affects the development and function of multiple organs and systems of the body. It is caused by mutations in the RBM10 gene, which is responsible for producing a protein that plays a crucial role in the development and function of various organs and tissues in the body.

Individuals with Tarp syndrome may experience a range of symptoms, including:

• Intellectual disability
• Delayed speech and language development
• Abnormal facial features
• Heart defects
• Abnormal skeletal development
• Respiratory problems
• Seizures

Diagnosis of Tarp Syndrome

Diagnosing Tarp syndrome can be challenging as it is a rare condition with varied symptoms that can mimic other medical conditions. However, doctors may suspect Tarp syndrome in individuals with specific symptoms and a family history of the disorder. A definitive diagnosis can be made through genetic testing to identify mutations in the RBM10 gene.

NGS Genetic DNA Test for Tarp Syndrome

Next-generation sequencing (NGS) is a powerful tool used for genetic testing that can sequence millions of DNA fragments simultaneously. It is an efficient and cost-effective method of identifying genetic mutations associated with various medical conditions, including Tarp syndrome.

The NGS genetic DNA test for Tarp syndrome involves analyzing the RBM10 gene to identify any mutations that may be responsible for causing the condition. The test can be performed using a blood sample or a saliva sample. The cost of the test in India is approximately INR 20,000.

Conclusion

Tarp syndrome is a rare genetic disorder that can have a significant impact on an individual's health and wellbeing. However, early diagnosis through genetic testing can help individuals receive appropriate medical care and support. The NGS genetic DNA test for Tarp syndrome is an efficient and cost-effective method of identifying mutations in the RBM10 gene and is available in India for approximately INR 20,000.

At DNA Labs India, we offer a wide range of genetic testing services, including NGS genetic DNA tests for various medical conditions. Our team of experts is committed to providing accurate and reliable genetic testing services to help individuals and families make informed decisions about their health.

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 RBM10 Gene Tarp syndrome NGS Genetic DNA Test