Walker-Warburg Syndrome (WWS) is a severe form of congenital muscular dystrophy associated with brain and eye abnormalities. This rare genetic disorder, affecting approximately 1 in every 100,000 live births, is characterized by muscle weakness, developmental delays, and structural brain defects. Understanding the symptoms of WWS is crucial for early diagnosis and intervention. DNA Labs UAE offers a comprehensive genetic test for the CRPPA gene, which has been linked to Walker-Warburg Syndrome, providing a valuable tool for families seeking answers.
The genetic test for Walker-Warburg Syndrome through the CRPPA gene is an essential step in diagnosing this complex condition. Priced at 4400 AED, this test is a critical resource for those exhibiting symptoms or with a family history of the disorder. For more information or to schedule a test, please visit our website.
Symptoms of Walker-Warburg Syndrome
Walker-Warburg Syndrome presents a range of symptoms, varying in severity among individuals. Recognizing these symptoms early can lead to a quicker diagnosis and the initiation of supportive treatments. Key symptoms include:
- Muscle Weakness: From birth, infants with WWS exhibit significant muscle weakness, impacting their ability to move and achieve developmental milestones.
- Brain Abnormalities: Structural issues in the brain, such as lissencephaly (smooth brain), hydrocephalus (excess fluid in the brain), and cerebellar malformations, are common.
- Eye Defects: Vision problems arise due to abnormalities in the eyes, including cataracts, glaucoma, and retinal dysplasia.
- Developmental Delays: Children with WWS often experience delays in reaching developmental milestones, including sitting up, walking, and speaking.
- Seizures: Epileptic seizures are a symptom for some individuals with WWS, further complicating their medical care.
Early detection and diagnosis of Walker-Warburg Syndrome are imperative for managing symptoms and improving the quality of life for affected individuals. The genetic test for the CRPPA gene offered by DNA Labs UAE is a vital tool in this process. By identifying the genetic underpinnings of WWS, families can access targeted support and interventions.
Understanding the CRPPA Gene Genetic Test
The CRPPA gene plays a crucial role in the development of Walker-Warburg Syndrome. Mutations in this gene are responsible for the majority of WWS cases. The genetic test for the CRPPA gene, available at DNA Labs UAE for 4400 AED, is a comprehensive analysis designed to detect these mutations. This test is particularly recommended for families with a history of WWS or for infants showing symptoms associated with the syndrome.
By choosing DNA Labs UAE for the CRPPA gene Walker-Warburg Syndrome genetic test, families gain access to advanced genetic testing technology, expert genetic counselors, and a supportive network to navigate the challenges of WWS. This test not only aids in the diagnosis but also provides families with crucial information for planning future pregnancies and understanding the condition better.
For more details on the CRPPA gene Walker-Warburg Syndrome genetic test or to schedule an appointment, please visit our website. Our team is dedicated to providing the support and information needed to navigate the complexities of genetic disorders like Walker-Warburg Syndrome.
