Short Description

NGS genetic DNA test detecets for variant and mutation detection in TFAP2A gene for Branchiooculofacial syndrome

PreTest Information

Clinical History of Patient who is going for TFAP2A Gene Branchiooculofacial syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TFAP2A Gene Branchiooculofacial syndrome NGS Genetic DNA Test gene TFAP2A

Detail Description

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TFAP2A Gene Branchiooculofacial Syndrome NGS Genetic DNA Test Cost INR 20000

TFAP2A Gene Branchiooculofacial Syndrome is a rare genetic disorder that affects the development of facial features, eyes, ears, and kidneys. It is caused by mutations in the TFAP2A gene, which provides instructions for making a protein that plays a critical role in the development of these structures.

The symptoms of TFAP2A Gene Branchiooculofacial Syndrome can vary widely from person to person, even among family members with the same mutation. Some common symptoms include:

• Cleft lip and/or palate
• Small or underdeveloped eyes (microphthalmia)
• Abnormally shaped ears
• Kidney abnormalities
• Facial asymmetry

Diagnosis of TFAP2A Gene Branchiooculofacial Syndrome can be confirmed through genetic testing. Next-generation sequencing (NGS) is a powerful tool that can detect mutations in the TFAP2A gene with high accuracy. At DNA Labs India, we offer NGS Genetic DNA Test for TFAP2A Gene Branchiooculofacial Syndrome at a cost of INR 20000.

If you suspect that you or a family member may have TFAP2A Gene Branchiooculofacial Syndrome, it is important to get tested as early as possible. Early diagnosis can help to ensure that appropriate medical care and support are provided.

Contact DNA Labs India today to schedule your NGS Genetic DNA Test for TFAP2A Gene Branchiooculofacial Syndrome.