Short Description

NGS genetic DNA test detecets for variant and mutation detection in BCL9L gene for Heterotaxy, visceral, BCL9L related

PreTest Information

Clinical History of Patient who is going for BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with BCL9L Gene Heterotaxy, visceral, BCL9L related NGS Genetic DNA Test gene BCL9L

Detail Description

BCL9L Gene Heterotaxy: Symptoms, Diagnosis, and BCL9L Related NGS Genetic DNA Test Cost

BCL9L gene is a vital gene that plays a crucial role in embryonic development, and any mutations in this gene can lead to various developmental abnormalities. One such abnormality is Heterotaxy, which is a rare genetic disorder characterized by the abnormal arrangement of internal organs in the chest and abdomen.

Symptoms of BCL9L Gene Heterotaxy

The symptoms of BCL9L Gene Heterotaxy can vary from person to person, depending on the severity and type of the disorder. Some of the common symptoms include:

• Abnormal arrangement of internal organs in the chest and abdomen
• Difficulty breathing or shortness of breath
• Heart defects
• Jaundice
• Delayed growth and development
• Recurrent infections

Diagnosis of BCL9L Gene Heterotaxy

The diagnosis of BCL9L Gene Heterotaxy involves a thorough physical examination and various diagnostic tests, including:

• CT scan
• MRI
• Echocardiogram
• Blood tests
• Genetic testing

Genetic testing is the most effective way to diagnose BCL9L Gene Heterotaxy. It involves analyzing the DNA of the patient to identify any mutations or abnormalities in the BCL9L gene. Next-generation sequencing (NGS) is a widely used genetic testing technique that can provide detailed information about genetic mutations.

BCL9L Related NGS Genetic DNA Test Cost

The cost of the BCL9L Related NGS Genetic DNA Test can vary depending on various factors, including the location, laboratory, and the type of test performed. However, the approximate cost of the BCL9L Related NGS Genetic DNA Test in India is INR 20,000.

Conclusion

BCL9L Gene Heterotaxy is a rare genetic disorder that can lead to various developmental abnormalities. Early diagnosis and treatment can significantly improve the quality of life of the affected individuals. Genetic testing, especially NGS, is the most effective way to diagnose BCL9L Gene Heterotaxy, and the cost of the test is affordable in India.

At DNA Labs India, we offer reliable and accurate genetic testing services to diagnose various genetic disorders, including BCL9L Gene Heterotaxy. Contact us to learn more about our genetic testing services.