HOXD13 Gene Syndactyly type 5 Genetic Test
Test Name: HOXD13 Gene Syndactyly type 5 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 HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test gene HOXD13
Test Details
The HOXD13 gene is associated with a condition called syndactyly type 5, also known as VACTERL syndrome. This genetic test is a Next-Generation Sequencing (NGS) test that examines the HOXD13 gene for any mutations or variations that may be responsible for causing syndactyly type 5.
Syndactyly type 5 is a rare genetic disorder characterized by the fusion of certain fingers or toes. It is typically inherited in an autosomal dominant manner, meaning that a mutation in one copy of the HOXD13 gene is sufficient to cause the condition.
The NGS genetic test for HOXD13 gene syndactyly type 5 involves sequencing the entire gene to identify any variations or mutations. This test can help confirm a diagnosis of syndactyly type 5 in individuals with characteristic symptoms and can also be used for carrier testing in family members of affected individuals.
It is important to note that genetic testing for syndactyly type 5 may not be available at all healthcare facilities and may require a referral to a specialized genetics clinic or laboratory. Additionally, genetic testing should be accompanied by genetic counseling to help individuals and families understand the results and implications of the test.
| Test Name | HOXD13 Gene Syndactyly type 5 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 HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with HOXD13 Gene Syndactyly type 5 NGS Genetic DNA Test gene HOXD13 |
| Test Details |
The HOXD13 gene is associated with a condition called syndactyly type 5, also known as VACTERL syndrome. This genetic test is a Next-Generation Sequencing (NGS) test that examines the HOXD13 gene for any mutations or variations that may be responsible for causing syndactyly type 5. Syndactyly type 5 is a rare genetic disorder characterized by the fusion of certain fingers or toes. It is typically inherited in an autosomal dominant manner, meaning that a mutation in one copy of the HOXD13 gene is sufficient to cause the condition. The NGS genetic test for HOXD13 gene syndactyly type 5 involves sequencing the entire gene to identify any variations or mutations. This test can help confirm a diagnosis of syndactyly type 5 in individuals with characteristic symptoms and can also be used for carrier testing in family members of affected individuals. It is important to note that genetic testing for syndactyly type 5 may not be available at all healthcare facilities and may require a referral to a specialized genetics clinic or laboratory. Additionally, genetic testing should be accompanied by genetic counseling to help individuals and families understand the results and implications of the test. |

