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WNT10B Gene Split-Handfoot Malformation Type 6 Genetic Test

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

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The WNT10B Gene Split-Hand/Foot Malformation Type 6 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the WNT10B gene that are associated with Split-Hand/Foot Malformation Type 6 (SHFM6). This condition is a rare genetic disorder characterized by the malformation or absence of certain fingers, toes, and occasionally long bones of the arms or legs. The test plays a crucial role in the early diagnosis and management of SHFM6, enabling healthcare providers to offer appropriate genetic counseling and consider potential treatments or interventions.

The testing process involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for specific genetic alterations in the WNT10B gene known to cause the disorder. This gene plays a significant role in the development of limbs and digits during embryonic growth.

The cost of the WNT10B Gene Split-Hand/Foot Malformation Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the advanced genetic analysis required to identify the specific mutations within the WNT10B gene. Patients considering this test are advised to consult with their healthcare providers to understand the implications of the results and to discuss the potential next steps in the management of the condition.

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WNT10B Gene Split-handfoot malformation type 6 Genetic Test

Are you or your loved ones experiencing symptoms of split-hand/foot malformation? DNA Labs UAE offers the WNT10B Gene Split-handfoot malformation type 6 Genetic Test at an affordable cost of AED 4400.0. This test can help diagnose and provide valuable information about this rare genetic disorder.

Test Details

The WNT10B gene is associated with split-hand/foot malformation type 6 (SHFM6), a condition characterized by incomplete development or absence of fingers and/or toes. Our NGS (Next-Generation Sequencing) technology allows for the simultaneous analysis of multiple genes or the entire genome, making it an efficient and comprehensive genetic testing method.

By analyzing the DNA sequence of the WNT10B gene, our NGS genetic testing can identify any mutations or variations that may be causing or contributing to the development of split-hand/foot malformation type 6. This information is crucial for confirming a diagnosis, providing genetic counseling, and guiding treatment options.

It’s important to note that genetic testing is typically recommended for individuals who have symptoms consistent with split-hand/foot malformation and a suspected genetic cause. Our team of expert pediatric doctors in the Genetics department can help determine if NGS genetic testing is appropriate for you or your loved ones.

Test Components and Price

The WNT10B Gene Split-handfoot malformation type 6 Genetic Test is priced at AED 4400.0. The test can be conducted using a blood sample, extracted DNA, or just one drop of blood on an FTA card.

Report Delivery

Once the sample is collected, the report will be delivered within 3 to 4 weeks. Our team ensures accurate and timely delivery of results.

Pre Test Information

Before undergoing the WNT10B Gene Split-handfoot malformation type 6 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 WNT10B gene. This information helps in better understanding the genetic inheritance pattern and potential risks.

Conclusion

If you or your loved ones are experiencing symptoms of split-hand/foot malformation, the WNT10B Gene Split-handfoot malformation type 6 Genetic Test offered by DNA Labs UAE can provide valuable insights. Our NGS technology allows for comprehensive analysis, enabling accurate diagnosis, genetic counseling, and personalized treatment options. Contact our Pediatrics department to determine if this test is appropriate for you and to get further information on the test and its implications.

Test Name WNT10B Gene Split-handfoot malformation type 6 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 WNT10B Gene Split-hand/foot malformation type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with WNT10B Gene Split-hand/foot malformation type 6 NGS Genetic DNA Test gene WNT10B
Test Details

The WNT10B gene is associated with a condition called split-hand/foot malformation type 6 (SHFM6). Split-hand/foot malformation is a rare genetic disorder characterized by the incomplete development or absence of fingers and/or toes.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or the entire genome. In the context of SHFM6, NGS genetic testing can be used to identify mutations or variations in the WNT10B gene.

By analyzing the DNA sequence of the WNT10B gene, NGS genetic testing can determine if there are any genetic changes that may be causing or contributing to the development of split-hand/foot malformation type 6. This information can be useful for confirming a diagnosis, providing genetic counseling, and guiding treatment options.

It’s important to note that genetic testing is typically recommended for individuals who have symptoms consistent with split-hand/foot malformation and a suspected genetic cause. A healthcare provider or genetic counselor can help determine if NGS genetic testing is appropriate and provide further information on the specific test and its implications.

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