Spinocerebellar ataxia type 12 (SCA12) is a rare, genetic disorder characterized by progressive loss of motor control and coordination. This condition is caused by mutations in the WWOX gene, which plays a critical role in the development and function of the nervous system. Understanding the symptoms of WWOX gene spinocerebellar ataxia type 12 and the availability of an autosomal recessive genetic test can significantly aid in the early diagnosis and management of this condition. DNA Labs UAE offers a comprehensive genetic test for this purpose.
Symptoms of WWOX Gene Spinocerebellar Ataxia Type 12
The symptoms of WWOX gene spinocerebellar ataxia type 12 typically manifest in adulthood, although the onset age can vary widely among individuals. The primary symptoms include:
- Motor Coordination Impairment: Difficulty with coordination and balance, including walking and tasks requiring fine motor skills.
- Tremors: Uncontrolled trembling or shaking, particularly in the hands.
- Dysarthria: Slurred or slow speech that can be difficult to understand.
- Nystagmus: Rapid, uncontrolled eye movements.
- Cognitive Decline: In some cases, individuals may experience problems with memory, planning, and decision-making.
As the disease progresses, these symptoms may worsen, leading to increased disability and dependence on others for daily activities.
Autosomal Recessive Genetic Test for WWOX Gene Spinocerebellar Ataxia Type 12
Understanding the genetic basis of SCA12 is crucial for accurate diagnosis and management. DNA Labs UAE offers an autosomal recessive genetic test specifically designed to detect mutations in the WWOX gene associated with spinocerebellar ataxia type 12. This test is a valuable tool for individuals with a family history of the condition or those exhibiting symptoms suggestive of SCA12.
The genetic test involves a simple blood draw or saliva sample, which is then analyzed in our state-of-the-art laboratory. Our team of genetic experts uses advanced sequencing techniques to identify any mutations in the WWOX gene that could indicate a predisposition to SCA12.
Cost of the Genetic Test
The cost of the WWOX gene spinocerebellar ataxia type 12 autosomal recessive genetic test at DNA Labs UAE is 4400 AED. While the cost may seem significant, early diagnosis and intervention can greatly improve the quality of life for individuals with SCA12 and potentially slow the progression of symptoms.
Conclusion
Spinocerebellar ataxia type 12 is a challenging condition, but understanding its genetic basis and recognizing the symptoms early can lead to better management and outcomes. DNA Labs UAE is committed to providing accurate and comprehensive genetic testing services, including the WWOX gene spinocerebellar ataxia type 12 autosomal recessive genetic test. For more information or to schedule a test, please visit our website at https://dnalabsuae.com/tests/wwox-gene-spinocerebellar-ataxia-type-12-autosomal-recessive-genetic-test/.
