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WNT7A Gene Fibular Aplasia or Hypoplasia Femoral Bowing and Poly- Syn- and Oligodactyly Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The “WNT7A Gene Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the WNT7A gene. These mutations are associated with a rare congenital condition characterized by a spectrum of limb abnormalities including the absence or underdevelopment of the fibula (fibular aplasia or hypoplasia), curvature of the femur (femoral bowing), and various abnormalities of the fingers and toes such as having too many (polydactyly), fused (syndactyly), or too few (oligodactyly). This comprehensive genetic test, costing 4400 AED, is crucial for accurate diagnosis, allowing for tailored treatment and management plans for affected individuals. DNA Labs UAE employs advanced genetic testing technologies to ensure precise and reliable results, aiding in the understanding and intervention of this complex condition.

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WNT7A Gene Fibular Aplasia or Hypoplasia Femoral Bowing and Poly-, Syn-, and Oligodactyly Genetic Test

At DNA Labs UAE, we offer the WNT7A Gene Fibular Aplasia or Hypoplasia Femoral Bowing and Poly-, Syn-, and Oligodactyly Genetic Test at a cost of AED 4400.0. This genetic test is designed to diagnose and provide valuable information about the condition associated with the WNT7A gene.

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

Prior to undergoing the WNT7A Gene Fibular Aplasia or Hypoplasia Femoral Bowing and Poly-, Syn-, and Oligodactyly Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by the condition associated with the WNT7A gene.

Test Details

The WNT7A gene is known to be associated with a condition characterized by fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly. Individuals with this condition may have an absence or underdevelopment of the fibula bone in the leg, bowing of the femur bone, and abnormalities in the digits of the hands and/or feet, such as extra, fused, or missing digits.

Our NGS (Next-Generation Sequencing) genetic testing method allows for the simultaneous analysis of multiple genes or the entire genome. In the case of WNT7A gene-related conditions, this genetic test can identify specific mutations or variants in the WNT7A gene that are associated with fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly. The results of this test can confirm a diagnosis, provide information about prognosis and inheritance pattern, and guide appropriate management and treatment options.

For more information or to schedule an appointment for the WNT7A Gene Fibular Aplasia or Hypoplasia Femoral Bowing and Poly-, Syn-, and Oligodactyly Genetic Test, please contact DNA Labs UAE.

Test Name WNT7A Gene Fibular aplasia or hypoplasia femoral bowing and poly- syn- and oligodactyly 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 Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT7A Gene Fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly NGS Genetic DNA Test gene WNT7A
Test Details

The WNT7A gene is associated with a condition called fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly. This condition is characterized by the absence or underdevelopment of the fibula bone in the leg, bowing of the femur bone, and the presence of extra, fused, or missing digits in the hands and/or feet.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of WNT7A gene-related conditions, NGS genetic testing can be used to identify specific mutations or variants in the WNT7A gene that are associated with fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly. This testing can help in confirming a diagnosis, providing information about the prognosis and inheritance pattern, and guiding appropriate management and treatment options.

SKU: TEST-4111 Category:

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