WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly Genetic Test
At DNA Labs UAE, we offer the WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly Genetic Test. This test is designed to diagnose and identify the genetic mutations or variants associated with Short-rib thoracic dysplasia type 11 with or without polydactyly (SRTD11).
Test Details
The WDR34 gene is specifically linked to the genetic disorder SRTD11, which is characterized by skeletal abnormalities, particularly affecting the ribs and long bones. This leads to a narrow thorax and short stature. Polydactyly, or extra fingers or toes, may also be present in individuals with this disorder.
Our NGS (Next-Generation Sequencing) technology allows us to analyze multiple genes simultaneously and detect any mutations or variants within the WDR34 gene that may be responsible for SRTD11. This genetic testing can confirm a diagnosis, provide information about the specific genetic mutation causing the disorder, and assist in genetic counseling for affected individuals and their families.
Test Components and Price
The cost of the WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly Genetic Test is AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card.
Report Delivery and Method
The report for this genetic test will be delivered within 3 to 4 weeks. We utilize NGS technology to analyze the WDR34 gene and identify any mutations or variants.
Test Type and Doctor
The WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly Genetic Test falls under the category of Dysmorphology. Our experienced pediatricians specialize in this field and will oversee the testing process.
Test Department and Pre-Test Information
This genetic test is conducted by our Genetics department. Before undergoing the WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly NGS Genetic DNA Test, it is essential to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by SRTD11.
Importance of Genetic Testing
Genetic testing for SRTD11 can not only confirm a diagnosis but also provide valuable information about the specific genetic mutation causing the disorder. This information can assist in genetic counseling for affected individuals and their families, aid in understanding the inheritance pattern of the disorder, and help make informed decisions regarding family planning and management of the condition.
It is crucial to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of genetic testing. They can also provide insights into the potential implications and limitations of the test results.
| Test Name | WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly 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 WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR34 Gene Short-rib thoracic dysplasia type 11 with or without polydactyly NGS Genetic DNA Test gene WDR34 |
| Test Details |
The WDR34 gene is associated with a genetic disorder called Short-rib thoracic dysplasia type 11 with or without polydactyly (SRTD11). This disorder is characterized by skeletal abnormalities, particularly affecting the ribs and long bones, leading to a narrow thorax and short stature. Polydactyly, or extra fingers or toes, may also be present. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify genetic mutations or variants that may be responsible for a particular disorder. In the case of SRTD11, NGS testing can be used to analyze the WDR34 gene and detect any mutations or variants that may be present. Genetic testing for SRTD11 can help confirm a diagnosis, provide information about the specific genetic mutation causing the disorder, and help with genetic counseling for affected individuals and their families. It can also aid in understanding the inheritance pattern of the disorder and assist in making informed decisions regarding family planning and management of the condition. It is important to consult with a healthcare professional or genetic counselor to discuss the appropriateness and availability of genetic testing, as well as the potential implications and limitations of the results. |
