WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly Genetic Test
At DNA Labs UAE, we offer the WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly Genetic Test. This test helps in diagnosing and understanding the symptoms of this genetic condition.
Test Components and Price
The test is priced at 4400.0 AED. The sample condition required for the test can be blood, extracted DNA, or one drop of blood on an FTA Card. The report delivery time is estimated to be 3 to 4 weeks. The test is conducted using NGS Technology, which refers to next-generation sequencing.
Test Type and Doctor
The WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly Genetic Test falls under the category of Dysmorphology. It is recommended to consult with a pediatrician for this test.
Test Department
The test is conducted in our Genetics department, ensuring accurate and reliable results.
Pre Test Information
Prior to taking the WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected by this genetic condition.
Test Details
The WDR35 gene is associated with a genetic condition known as short-rib thoracic dysplasia type 7 (SRTD7) with or without polydactyly. SRTD7 is a rare autosomal recessive disorder characterized by skeletal abnormalities such as short ribs, a narrow thorax, and shortened long bones. It may also be accompanied by additional features like polydactyly, cleft palate, and kidney abnormalities.
NGS genetic testing, which stands for next-generation sequencing, is used to analyze multiple genes simultaneously. In the context of SRTD7, NGS genetic testing involves sequencing the WDR35 gene to identify any disease-causing mutations or variants. This can help confirm a clinical diagnosis, provide genetic counseling, and guide treatment decisions.
If you suspect that you or someone you know may have SRTD7 or if there is a family history of the condition, it is highly recommended to consult with a healthcare professional or a genetic counselor. They can provide more information and guidance regarding genetic testing options.
| Test Name | WDR35 Gene Short-rib thoracic dysplasia type 7 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 WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR35 Gene Short-rib thoracic dysplasia type 7 with or without polydactyly NGS Genetic DNA Test gene WDR35 |
| Test Details | The WDR35 gene is associated with a genetic condition called short-rib thoracic dysplasia type 7 (SRTD7) with or without polydactyly. SRTD7 is a rare autosomal recessive disorder characterized by skeletal abnormalities, including short ribs, a narrow thorax, and shortened long bones. It may also be associated with additional features such as polydactyly (extra fingers or toes), cleft palate, and kidney abnormalities. NGS genetic testing refers to next-generation sequencing, a high-throughput method used to analyze multiple genes simultaneously. In the context of SRTD7, NGS genetic testing involves sequencing the WDR35 gene to identify any disease-causing mutations or variants. This can help in confirming a clinical diagnosis, providing genetic counseling, and potentially guiding treatment decisions. If you suspect that you or someone you know may have SRTD7 or if there is a family history of the condition, it is recommended to consult with a healthcare professional or a genetic counselor who can provide more information and guidance regarding genetic testing options. |
