WNT7A Gene Ulna and Fibula Absence with Severe Limb Deficiency Genetic Test
At DNA Labs UAE, we offer the WNT7A Gene Ulna and Fibula Absence with Severe Limb Deficiency Genetic Test. This test helps in diagnosing individuals with the absence or underdevelopment of the ulna bone in the forearm and the fibula bone in the lower leg, along with severe limb deficiency.
Test Components and Price
Test Name: WNT7A Gene Ulna and Fibula Absence of with Severe Limb Deficiency Genetic Test
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 WNT7A Gene Ulna and Fibula Absence of with Severe Limb Deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT7A Gene Ulna and Fibula Absence of with Severe Limb Deficiency NGS Genetic DNA Test gene WNT7A.
Test Details
WNT7A gene ulna and fibula absence of with severe limb deficiency is a genetic condition characterized by the absence or underdevelopment of the ulna bone in the forearm and the fibula bone in the lower leg, along with severe limb deficiency. This condition is caused by mutations in the WNT7A gene. The WNT7A gene provides instructions for producing a protein that is involved in the development of limbs during embryonic development. Mutations in this gene disrupt the normal development of the ulna and fibula bones, leading to their absence or incomplete formation. This results in severe limb deficiency, where the affected individuals have shortened or missing forearms and lower legs.
NGS (Next-Generation Sequencing) genetic testing can be used to identify mutations in the WNT7A gene. This testing method allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of the genetic variations that may be responsible for the condition. Genetic testing can help in confirming the diagnosis of WNT7A gene ulna and fibula absence with severe limb deficiency and can also assist in genetic counseling for affected individuals and their families. It can provide information about the likelihood of passing the condition on to future generations and help in making informed decisions regarding family planning.
It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the individual’s specific situation.
| Test Name | WNT7A Gene Ulna and fibula absence of with severe limb deficiency 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 WNT7A Gene Ulna and fibula, absence of, with severe limb deficiency NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT7A Gene Ulna and fibula, absence of, with severe limb deficiency NGS Genetic DNA Test gene WNT7A |
| Test Details |
WNT7A gene ulna and fibula, absence of, with severe limb deficiency is a genetic condition characterized by the absence or underdevelopment of the ulna bone in the forearm and the fibula bone in the lower leg, along with severe limb deficiency. This condition is caused by mutations in the WNT7A gene. The WNT7A gene provides instructions for producing a protein that is involved in the development of limbs during embryonic development. Mutations in this gene disrupt the normal development of the ulna and fibula bones, leading to their absence or incomplete formation. This results in severe limb deficiency, where the affected individuals have shortened or missing forearms and lower legs. NGS (Next-Generation Sequencing) genetic testing can be used to identify mutations in the WNT7A gene. This testing method allows for the simultaneous analysis of multiple genes, providing a comprehensive assessment of the genetic variations that may be responsible for the condition. Genetic testing can help in confirming the diagnosis of WNT7A gene ulna and fibula absence with severe limb deficiency and can also assist in genetic counseling for affected individuals and their families. It can provide information about the likelihood of passing the condition on to future generations and help in making informed decisions regarding family planning. It is important to note that genetic testing should be performed and interpreted by a qualified healthcare professional or genetic counselor who can provide appropriate guidance and support based on the individual’s specific situation. |
