Symptoms and Testing information for WNT4 Gene SERKAL syndrome Genetic Test

Symptoms and Testing information for WNT4 Gene SERKAL syndrome Genetic Test

In the realm of medical genetics, the exploration of specific gene mutations and their associated syndromes has opened new avenues for diagnosis and treatment. One such breakthrough has been in the understanding of the WNT4 gene and its link to SERKAL syndrome. DNA Labs UAE stands at the forefront of this research, offering a comprehensive genetic test designed to diagnose this rare condition. This article delves into the symptoms associated with SERKAL syndrome, the significance of the WNT4 gene, and the details surrounding the genetic test available at DNA Labs UAE, including its cost.

Symptoms of SERKAL Syndrome

SERKAL syndrome, stemming from mutations in the WNT4 gene, manifests through a variety of symptoms, primarily affecting the reproductive and renal systems. The syndrome is characterized by a range of clinical features that can vary significantly among affected individuals. Key symptoms include:

  • Sexual Development Disorders: Individuals with SERKAL syndrome may experience abnormal sexual development. This can manifest as ambiguous genitalia or discrepancies between the external genitals and the internal reproductive organs.
  • Renal Anomalies: Kidney issues are a common symptom, ranging from mild renal dysplasia to severe renal agenesis, where one or both kidneys fail to develop.
  • Müllerian Duct Anomalies: Affected females may have abnormalities in the development of the Müllerian ducts, leading to issues with the uterus and fallopian tubes, which can impact fertility.
  • Skeletal Abnormalities: Some individuals may exhibit skeletal abnormalities, including hip dysplasia or vertebral anomalies.
  • Secondary Health Issues: Other symptoms can include recurrent urinary tract infections, hypertension, and in some cases, progressive renal failure.

Early diagnosis of SERKAL syndrome is crucial for managing these symptoms and improving the quality of life for affected individuals.

The Role of the WNT4 Gene

The WNT4 gene plays a pivotal role in the development of the reproductive and renal systems. It is involved in the signaling pathways that guide the formation of these organs during fetal development. Mutations in the WNT4 gene disrupt these pathways, leading to the manifestations of SERKAL syndrome. Understanding the function of the WNT4 gene is essential for diagnosing and treating conditions associated with its mutations.

WNT4 Gene SERKAL Syndrome Genetic Test at DNA Labs UAE

DNA Labs UAE offers a specialized genetic test for diagnosing SERKAL syndrome, targeting mutations in the WNT4 gene. This test is designed for individuals who exhibit symptoms of the syndrome or have a family history of related conditions. The test involves a simple blood sample from which DNA is extracted and analyzed for specific mutations in the WNT4 gene.

The cost of the WNT4 Gene SERKAL Syndrome Genetic Test is 4400 AED. This comprehensive analysis provides crucial information for the diagnosis and management of SERKAL syndrome, enabling targeted interventions and genetic counseling for affected families.

For more information or to schedule a test, please visit DNA Labs UAE.

Conclusion

Understanding the symptoms and genetic basis of SERKAL syndrome is essential for effective diagnosis and management. The WNT4 Gene SERKAL Syndrome Genetic Test offered by DNA Labs UAE represents a critical tool in this process, providing individuals and families with the information needed to navigate the challenges associated with this condition. With advancements in genetic testing, there is hope for improved outcomes and support for those affected by SERKAL syndrome.

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