Williams-Beuren Syndrome (WBS) is a rare genetic disorder caused by a deletion of several genes on chromosome 7, specifically at the 7q11.23 locus. This complex condition is characterized by a range of medical and developmental issues, including cardiovascular disease, developmental delays, and distinctive facial features. Understanding the symptoms of Williams-Beuren Syndrome is crucial for early diagnosis and management of the condition. At DNA Labs UAE, we offer a comprehensive genetic test for the 7q11.23 gene deletion associated with Williams-Beuren Syndrome, priced at 4400 AED.
Understanding Williams-Beuren Syndrome
Williams-Beuren Syndrome affects many parts of the body and is known for its unique combination of medical and developmental features. Individuals with WBS often have cardiovascular diseases, particularly narrowing of the arteries, which can lead to elevated blood pressure and heart problems. Developmental delays are common, including challenges with learning disabilities, although affected individuals often have strong verbal skills and are highly social. Additionally, people with WBS tend to have a distinctive facial appearance, including a wide mouth, full lips, a small upturned nose, and widely spaced teeth.
Symptoms of Williams-Beuren Syndrome
The symptoms of Williams-Beuren Syndrome vary widely among individuals but generally include:
- Cardiovascular problems, such as supravalvular aortic stenosis
- Developmental delays and learning challenges
- Unique facial features, including a wide mouth and full lips
- Hypercalcemia (elevated levels of calcium in the blood)
- Musculoskeletal problems, such as joint stiffness and abnormalities in gait
- Behavioral characteristics, including anxiety, phobias, and an overly friendly demeanor
Early diagnosis and intervention are crucial for managing the symptoms of Williams-Beuren Syndrome and improving the quality of life for those affected. This makes genetic testing an invaluable tool for families and physicians.
Genetic Test for Williams-Beuren Syndrome at DNA Labs UAE
At DNA Labs UAE, we offer a specific genetic test designed to detect the deletion of genes at the 7q11.23 locus, confirming the diagnosis of Williams-Beuren Syndrome. Priced at 4400 AED, this test is a critical step in the diagnostic process, providing families and healthcare providers with the information needed to tailor care and interventions for individuals with WBS.
Our state-of-the-art laboratory is equipped with the latest in genetic testing technology, ensuring accurate and reliable results. Our team of genetic counselors and specialists are also available to provide support and guidance throughout the testing process.
For more information about the Chr. 7q11.23 Gene Williams-Beuren Syndrome Genetic Test and to schedule a consultation, please visit DNA Labs UAE.
Conclusion
Williams-Beuren Syndrome is a complex genetic condition that requires early diagnosis and comprehensive management. The symptoms of WBS can vary widely, but with the right interventions, individuals with this syndrome can lead fulfilling lives. Genetic testing plays a crucial role in the diagnosis of WBS, offering families and healthcare providers the information needed to make informed decisions about care. At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services, including the test for Williams-Beuren Syndrome, to support the health and well-being of individuals and families affected by this condition.
