Spinocerebellar ataxia type 21 (SCA21) is a rare, inherited neurological disorder characterized by progressive problems with movement. This condition is caused by mutations in the TMEM240 gene, which plays a critical role in the functioning of the cerebellum, the part of the brain that controls coordination and balance. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive TMEM240 Gene Spinocerebellar Ataxia Type 21 Autosomal Dominant Genetic Test, priced at 4400 AED, to aid in the diagnosis of this condition. For more information, please visit our website.
Symptoms of TMEM240 Gene Spinocerebellar Ataxia Type 21
Spinocerebellar ataxia type 21 is a progressive disorder, meaning that symptoms worsen over time. The onset of symptoms typically occurs in adulthood, but the age of onset and the severity of symptoms can vary widely among affected individuals. The following are some of the common symptoms associated with SCA21:
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Difficulty with coordination and balance (ataxia), leading to frequent falls
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Slow and slurred speech (dysarthria)
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Difficulty swallowing (dysphagia)
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Slow eye movements or difficulty controlling eye movements
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Weakness in the legs and, later on, in the arms
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Tremors or involuntary muscle movements
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Cognitive impairment, although this is less common
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Changes in personality and behavior
It is important to note that the presence and severity of symptoms can vary significantly from one person to another, even among members of the same family. This variability can sometimes make the condition challenging to diagnose without genetic testing.
Importance of Genetic Testing for TMEM240 Gene Spinocerebellar Ataxia Type 21
Genetic testing plays a crucial role in the diagnosis of spinocerebellar ataxia type 21. The TMEM240 Gene Spinocerebellar Ataxia Type 21 Autosomal Dominant Genetic Test offered by DNA Labs UAE is specifically designed to detect mutations in the TMEM240 gene that are responsible for the condition. This test is not only important for confirming the diagnosis but also for understanding the risk of passing the condition on to future generations.
Early diagnosis through genetic testing can also help in managing the symptoms more effectively. While there is currently no cure for SCA21, interventions such as physical therapy, speech therapy, and occupational therapy can significantly improve the quality of life for those affected. Genetic counseling is also recommended for individuals and families to understand the implications of the test results.
Cost of the TMEM240 Gene Spinocerebellar Ataxia Type 21 Genetic Test
The cost of the TMEM240 Gene Spinocerebellar Ataxia Type 21 Autosomal Dominant Genetic Test at DNA Labs UAE is 4400 AED. This cost includes the genetic test itself, as well as pre-test and post-test counseling sessions to help individuals understand their results and the next steps to take.
For more detailed information about the test and to schedule an appointment, please visit DNA Labs UAE. Our team of experts is dedicated to providing you with the support and guidance you need throughout the testing process.
