In the realm of genetic testing and diagnosis, the advancement of technology has paved the way for identifying and understanding a plethora of genetic disorders that affect individuals from birth. One such condition is Williams Syndrome, a rare genetic disorder characterized by a unique set of symptoms and challenges. DNA Labs UAE, a leading genetic laboratory in the United Arab Emirates, offers a comprehensive testing solution for this condition: the FISH – Microdeletion Detection for Williams Syndrome Test. This test, priced at 1510 AED, is a critical tool in diagnosing Williams Syndrome, enabling early intervention and support for affected individuals and their families.
Understanding Williams Syndrome
Williams Syndrome is a genetic condition caused by the deletion of genetic material on chromosome 7. This deletion affects the elastin gene, among others, leading to a constellation of physical, developmental, and emotional symptoms. Individuals with Williams Syndrome often have distinctive facial features, such as a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips. Beyond physical characteristics, those with Williams Syndrome typically exhibit heart and blood vessel issues, developmental delays, learning challenges, and a unique personality profile that includes being overly friendly and lacking social inhibition.
Symptoms of Williams Syndrome
The symptoms of Williams Syndrome are diverse and can vary significantly from one individual to another. However, some common signs include:
- Distinctive facial features as described above
- Heart and blood vessel problems, especially supravalvular aortic stenosis
- Hypercalcemia (elevated blood calcium levels), which can cause irritability and colic-like symptoms in infants
- Developmental delays and learning challenges
- Unique personality characteristics, including being highly sociable and empathetic
- Sensitivity to loud noises
- Problems with spatial relations and fine motor skills
FISH – Microdeletion Detection for Williams Syndrome Test
At DNA Labs UAE, the FISH (Fluorescence In Situ Hybridization) – Microdeletion Detection test is a specialized genetic test designed to identify the deletion of material on chromosome 7, which indicates Williams Syndrome. This test is not only crucial for diagnosis but also for understanding the extent of the deletion, which can provide insight into the potential severity of the condition and guide treatment and support plans. The test, which costs 1510 AED, is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring accuracy and reliability of results.
Why Choose DNA Labs UAE?
DNA Labs UAE stands at the forefront of genetic testing in the Middle East, offering a wide range of services from ancestry testing to complex genetic disorder screenings. The lab is equipped with the latest technology and staffed by experts in the field of genetics, ensuring that every test, including the FISH – Microdeletion Detection for Williams Syndrome Test, is conducted with the utmost precision and care. Furthermore, DNA Labs UAE is committed to providing support and counseling to families navigating the challenges of genetic disorders, making it a comprehensive resource for those in need.
Conclusion
Williams Syndrome, though rare, can significantly impact the lives of affected individuals and their families. Early detection through the FISH – Microdeletion Detection for Williams Syndrome Test offered by DNA Labs UAE is crucial for accessing interventions and supports that can improve quality of life. With a cost of 1510 AED, this test is an invaluable tool in the journey towards understanding and managing Williams Syndrome. For more information, visit DNA Labs UAE.
