LHFPL5 Gene Deafness Autosomal Recessive Type 67 Genetic Test
At DNA Labs UAE, we offer the LHFPL5 Gene Deafness Autosomal Recessive Type 67 Genetic Test. This test is designed to diagnose individuals with suspected LHFPL5 gene deafness, autosomal recessive type 67 and provide information about the inheritance pattern of the condition.
Test Details
LHFPL5 gene deafness, autosomal recessive type 67 is a specific type of deafness that is caused by mutations in the LHFPL5 gene. This type of deafness is inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated for the condition to be present.
Our test uses NGS (Next-Generation Sequencing) technology, which allows us to analyze multiple genes simultaneously. In the case of LHFPL5 gene deafness, autosomal recessive type 67, NGS genetic testing can identify mutations in the LHFPL5 gene that may be causing the deafness.
In addition to diagnosing individuals with suspected LHFPL5 gene deafness, autosomal recessive type 67, our test can also be used for carrier testing. This can help individuals determine if they carry a mutation in the LHFPL5 gene and may be at risk of passing it on to their children.
Test Components and Price
The LHFPL5 Gene Deafness Autosomal Recessive Type 67 Genetic Test is priced at 4400.0 AED. The test can be conducted using either blood or extracted DNA, or with just one drop of blood on an FTA Card.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The test is performed using NGS technology, which ensures accurate and reliable results.
Test Type and Doctor
The LHFPL5 Gene Deafness Autosomal Recessive Type 67 Genetic Test falls under the category of Ear Nose Throat Disorders. It is recommended to consult an ENT Doctor for this test.
Test Department and Pre Test Information
The LHFPL5 Gene Deafness Autosomal Recessive Type 67 Genetic Test is conducted in our Genetics department. Before taking the test, it is important to provide the clinical history of the patient who is going for the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN32.
It is crucial to note that genetic testing for LHFPL5 gene deafness, autosomal recessive type 67 should be done in consultation with a healthcare professional or genetic counselor who can provide guidance and interpretation of the results.
| Test Name | LHFPL5 Gene Deafness autosomal recessive type 67 Genetic Test |
|---|---|
| Components | |
| Price | 4400.0 AED |
| Sample Condition | Blood or Extracted DNA or One drop Blood on FTA Card |
| Report Delivery | 3 to 4 Weeks |
| Method | NGS Technology |
| Test type | Ear Nose Throat Disorders |
| Doctor | ENT Doctor |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN32 |
| Test Details | LHFPL5 gene deafness, autosomal recessive type 67 is a specific type of deafness that is caused by mutations in the LHFPL5 gene. This type of deafness is inherited in an autosomal recessive manner, meaning that both copies of the gene must be mutated for the condition to be present. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the case of LHFPL5 gene deafness, autosomal recessive type 67, NGS genetic testing can identify mutations in the LHFPL5 gene that may be causing the deafness. This type of genetic testing can be useful in diagnosing individuals with suspected LHFPL5 gene deafness, autosomal recessive type 67, as well as in providing information about the inheritance pattern of the condition. It can also be used for carrier testing, which can help individuals determine if they carry a mutation in the LHFPL5 gene and may be at risk of passing it on to their children. It is important to note that genetic testing for LHFPL5 gene deafness, autosomal recessive type 67 should be done in consultation with a healthcare professional or genetic counselor who can provide guidance and interpretation of the results. |
