Short Description

NGS genetic DNA test detecets for variant and mutation detection in DLX5 gene for Split-hand/foot malformation type 1 with sensorineural hearing loss

PreTest Information

Clinical History of Patient who is going for DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic DNA Test gene DLX5

Detail Description

DLX5 Gene Split-hand/foot malformation type 1 with sensorineural hearing loss NGS Genetic DNA Test cost INR:20000 symptoms diagnosis

Split-hand/foot malformation type 1 (SHFM1) is a genetic condition that affects the development of limbs, resulting in split or missing fingers or toes. This condition can also cause sensorineural hearing loss, which affects the ability to hear sounds.

The DLX5 gene is responsible for producing a protein that plays a crucial role in limb development. Mutations in this gene can cause SHFM1 with sensorineural hearing loss.

Symptoms of DLX5 Gene SHFM1 with Sensorineural Hearing Loss

The symptoms of DLX5 Gene SHFM1 with sensorineural hearing loss can vary widely between individuals. Some common symptoms include:

• Split or missing fingers or toes
• Abnormal bone growth in the hands or feet
• Shortened digits
• Delayed speech development
• Sensorineural hearing loss

Diagnosis of DLX5 Gene SHFM1 with Sensorineural Hearing Loss

Diagnosis of DLX5 Gene SHFM1 with sensorineural hearing loss typically involves a physical exam and genetic testing. A doctor may perform X-rays to examine the bones in the hands and feet and hearing tests to assess the severity of hearing loss. Genetic testing can confirm the presence of mutations in the DLX5 gene.

NGS Genetic DNA Test for DLX5 Gene SHFM1 with Sensorineural Hearing Loss

NGS Genetic DNA Test for DLX5 Gene SHFM1 with sensorineural hearing loss is a genetic test that uses Next-Generation Sequencing (NGS) technology to analyze the DLX5 gene for mutations. This test can help confirm a diagnosis of SHFM1 with sensorineural hearing loss and can also provide important information about the severity of the condition and the likelihood of passing it on to future generations.

Cost of NGS Genetic DNA Test for DLX5 Gene SHFM1 with Sensorineural Hearing Loss

The cost of NGS Genetic DNA Test for DLX5 Gene SHFM1 with sensorineural hearing loss in India is INR 20,000. This cost may vary depending on the testing facility and any additional services that may be required.

Conclusion

DLX5 Gene SHFM1 with sensorineural hearing loss is a rare genetic condition that can cause split or missing fingers or toes and hearing loss. Genetic testing, including NGS Genetic DNA Test, can help diagnose this condition and provide important information about its severity and likelihood of passing it on to future generations. If you are experiencing symptoms of SHFM1 with sensorineural hearing loss, speak to your doctor about genetic testing and treatment options.

At DNA Labs India, we offer a wide range of genetic tests, including NGS Genetic DNA Test for DLX5 Gene SHFM1 with sensorineural hearing loss. Contact us to learn more about our testing services and how we can help you get the answers you need.