TBX5 Gene Holt-Oram syndrome Genetic Test
At DNA Labs UAE, we offer the TBX5 Gene Holt-Oram syndrome Genetic Test for individuals who may be at risk of this rare genetic disorder. This test analyzes the TBX5 gene for mutations associated with Holt-Oram syndrome, a condition that affects the development of the heart and upper limbs.
Test Details
The TBX5 Gene Holt-Oram syndrome Genetic Test is a type of genetic test that utilizes Next-Generation Sequencing (NGS) technology. NGS allows for the analysis of multiple genes simultaneously, providing a comprehensive assessment of the TBX5 gene.
Components and Price
The cost of the TBX5 Gene Holt-Oram syndrome Genetic Test is 4400.0 AED. The test can be performed on blood samples or extracted DNA. Alternatively, one drop of blood can be collected on an FTA Card for testing.
Report Delivery
The report for the TBX5 Gene Holt-Oram syndrome Genetic Test is typically delivered within 3 to 4 weeks.
Test Type and Department
The TBX5 Gene Holt-Oram syndrome Genetic Test falls under the category of Dysmorphology. It is conducted by our expert team in the Genetics department.
Pre Test Information
Prior to undergoing the TBX5 Gene Holt-Oram syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected by Holt-Oram syndrome.
About Holt-Oram Syndrome
Holt-Oram syndrome is a rare genetic disorder that affects the development of the heart and upper limbs. It is caused by mutations in the TBX5 gene, which plays a crucial role in the development of these structures during embryogenesis.
NGS Technology
Next-Generation Sequencing (NGS) is a high-throughput sequencing technology used in the TBX5 Gene Holt-Oram syndrome Genetic Test. It allows for the sequencing of the TBX5 gene and identification of potential mutations or variations associated with Holt-Oram syndrome.
Diagnosis and Testing
The TBX5 Gene Holt-Oram syndrome Genetic Test can be used to diagnose Holt-Oram syndrome in individuals who exhibit symptoms such as heart defects and skeletal abnormalities in the upper limbs. It can also be used for carrier testing in individuals with a family history of the condition, as well as for prenatal testing in families at risk of having an affected child.
Benefits of the Test
The results of the TBX5 Gene Holt-Oram syndrome Genetic Test can help healthcare professionals confirm a diagnosis of Holt-Oram syndrome. It also enables them to provide genetic counseling to affected individuals and their families, and guide appropriate medical management and treatment options.
Choose DNA Labs UAE for accurate and reliable genetic testing. Contact us today to schedule an appointment or learn more about our services.
| Test Name | TBX5 Gene Holt-Oram syndrome 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 | Dysmorphology |
| Doctor | Pediatrics |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for TBX5 Gene Holt-Oram syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TBX5 Gene Holt-Oram syndrome NGS Genetic DNA Test gene TBX5 |
| Test Details |
The TBX5 gene Holt-Oram syndrome NGS genetic test is a type of genetic test that analyzes the TBX5 gene for mutations associated with Holt-Oram syndrome. Holt-Oram syndrome is a rare genetic disorder that affects the development of the heart and upper limbs. It is caused by mutations in the TBX5 gene, which plays a crucial role in the development of the heart and upper limbs during embryogenesis. NGS stands for Next-Generation Sequencing, which is a high-throughput sequencing technology that allows for the analysis of multiple genes simultaneously. In the case of the TBX5 gene Holt-Oram syndrome NGS genetic test, NGS technology is used to sequence the TBX5 gene and identify any potential mutations or variations that may be associated with Holt-Oram syndrome. This genetic test can be used to diagnose Holt-Oram syndrome in individuals who exhibit symptoms of the condition, such as heart defects and skeletal abnormalities in the upper limbs. It can also be used for carrier testing in individuals with a family history of Holt-Oram syndrome, as well as for prenatal testing in families at risk of having a child with the condition. The results of the TBX5 gene Holt-Oram syndrome NGS genetic test can help healthcare professionals confirm a diagnosis of Holt-Oram syndrome, provide genetic counseling to affected individuals and their families, and guide appropriate medical management and treatment options. |
