Short Description

NGS genetic DNA test detecets for variant and mutation detection in AIFM1 gene for Deafness, X-linked type 5

PreTest Information

Clinical History of Patient who is going for SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SLC52A2 Gene Brown-Vialetto-Van Laere syndrome type 2 NGS Genetic DNA Test gene SLC52A14

Detail Description

AIFM1 Gene Deafness: Understanding X-linked Type 5 NGS Genetic DNA Test

Deafness is a condition that affects millions of people worldwide. It can be caused by different factors, including genetic mutations. One such genetic mutation is the AIFM1 gene, which is associated with X-linked type 5 deafness. This condition affects males more than females, and it is estimated that 1 in 10,000 people are affected by this condition.

The AIFM1 gene provides instructions for making a protein called apoptosis-inducing factor (AIF). This protein plays a crucial role in the mitochondria, which are the energy-producing structures within cells. When the AIFM1 gene is mutated, it can disrupt the function of the mitochondria and cause hearing loss.

Symptoms of AIFM1 Gene Deafness

The symptoms of AIFM1 gene deafness can vary from person to person. In some cases, the hearing loss may be mild, while in others, it can be severe. The following are some of the common symptoms of AIFM1 gene deafness:

• Difficulty hearing high-pitched sounds
• Trouble understanding speech, especially in noisy environments
• Progressive hearing loss
• Tinnitus (ringing in the ears)

Diagnosis of AIFM1 Gene Deafness

If you or someone you know is experiencing symptoms of AIFM1 gene deafness, it is essential to seek medical attention. A doctor or an audiologist may conduct a hearing test to determine the extent of the hearing loss. Additionally, a genetic test may be recommended to confirm the diagnosis of AIFM1 gene deafness.

X-linked Type 5 NGS Genetic DNA Test

X-linked type 5 deafness is caused by a mutation in the AIFM1 gene. A Next-Generation Sequencing (NGS) genetic DNA test can be used to detect this mutation. This test analyzes the DNA sequence of the AIFM1 gene to identify any mutations that may be present.

The X-linked type 5 NGS genetic DNA test is a reliable and accurate test that can confirm the diagnosis of AIFM1 gene deafness. It is a non-invasive test that requires a small blood or saliva sample.

Cost of X-linked Type 5 NGS Genetic DNA Test

The cost of the X-linked type 5 NGS genetic DNA test for AIFM1 gene deafness in India is approximately INR 20,000. The cost may vary depending on the laboratory and the location.

Conclusion

If you or someone you know is experiencing symptoms of AIFM1 gene deafness, it is essential to seek medical attention. X-linked type 5 NGS genetic DNA test can confirm the diagnosis of AIFM1 gene deafness. DNA Labs India offers reliable and accurate genetic testing services for AIFM1 gene deafness at an affordable cost. Contact us today to schedule an appointment.

Remember, early detection and intervention can significantly improve the quality of life for individuals with AIFM1 gene deafness.