WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly Genetic Test
Test Name: WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
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 WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly NGS Genetic DNA Test gene WDR19
Test Details
The WDR19 gene is associated with a genetic condition called short-rib thoracic dysplasia type 5 with or without polydactyly (SRTD5). This condition is characterized by skeletal abnormalities, particularly affecting the ribs and long bones of the arms and legs. Polydactyly, which is the presence of extra fingers or toes, may also be present in some individuals.
NGS genetic testing refers to next-generation sequencing, a high-throughput method used to analyze multiple genes simultaneously. In the context of SRTD5, NGS genetic testing can be used to identify mutations or variations in the WDR19 gene that may be responsible for the condition. By identifying specific genetic changes, NGS testing can provide a definitive diagnosis of SRTD5.
This information can be valuable for understanding the underlying cause of the condition, predicting disease progression, and guiding treatment options and management strategies. Additionally, genetic testing may also provide information about the likelihood of passing on the condition to future generations.
It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.
| Test Name | WDR19 Gene Short-rib thoracic dysplasia type 5 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 WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WDR19 Gene Short-rib thoracic dysplasia type 5 with or without polydactyly NGS Genetic DNA Test gene WDR19 |
| Test Details |
The WDR19 gene is associated with a genetic condition called short-rib thoracic dysplasia type 5 with or without polydactyly (SRTD5). This condition is characterized by skeletal abnormalities, particularly affecting the ribs and long bones of the arms and legs. Polydactyly, which is the presence of extra fingers or toes, may also be present in some individuals. NGS genetic testing refers to next-generation sequencing, a high-throughput method used to analyze multiple genes simultaneously. In the context of SRTD5, NGS genetic testing can be used to identify mutations or variations in the WDR19 gene that may be responsible for the condition. By identifying specific genetic changes, NGS testing can provide a definitive diagnosis of SRTD5. This information can be valuable for understanding the underlying cause of the condition, predicting disease progression, and guiding treatment options and management strategies. Additionally, genetic testing may also provide information about the likelihood of passing on the condition to future generations. It is important to note that genetic testing should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance. |
