Spinocerebellar ataxia type 10 (SCA10) is a rare genetic disorder that affects the central nervous system, leading to a progressive loss of muscle coordination and balance. This condition is caused by mutations in the ANO10 gene and is inherited in an autosomal recessive pattern. Understanding the symptoms and genetic basis of SCA10 is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for SCA10, aiding in the accurate diagnosis of this condition.
Symptoms of ANO10 Gene Spinocerebellar Ataxia Type 10
The symptoms of SCA10 can vary widely among affected individuals but typically include a progressive loss of coordination (ataxia) that begins in adulthood. The key symptoms associated with SCA10 include:
- Gait Ataxia: Difficulty in walking, leading to a wide-based, unsteady gait.
- Limb Ataxia: Lack of coordination in the arms and legs, leading to clumsiness and unsteady movements.
- Dysarthria: Slurred or slow speech resulting from an inability to control the muscles used in speech.
- Oculomotor Dysfunctions: Difficulty in controlling eye movements, which can lead to double vision or involuntary eye movements.
- Cognitive Impairments: Mild to moderate difficulties with memory, planning, and decision-making.
As SCA10 progresses, individuals may also experience muscle weakness, difficulty swallowing (dysphagia), and a decline in fine motor skills. The severity and progression of symptoms can vary, but they typically worsen over time, leading to significant disability.
ANO10 Gene Spinocerebellar Ataxia Type 10 Autosomal Recessive Genetic Test
DNA Labs UAE offers a genetic test specifically designed to diagnose SCA10 by identifying mutations in the ANO10 gene. This test is crucial for individuals who have a family history of SCA10 or who exhibit symptoms consistent with the condition. Early and accurate diagnosis can facilitate better management and treatment options for affected individuals.
The genetic test for SCA10 at DNA Labs UAE involves a simple blood draw or saliva sample. The sample is then analyzed in our state-of-the-art laboratory using advanced genetic sequencing technologies to detect mutations in the ANO10 gene. The process is highly accurate and provides a definitive diagnosis of SCA10.
The cost of the ANO10 gene spinocerebellar ataxia type 10 autosomal recessive genetic test is 4400 AED. This investment covers the comprehensive analysis and detailed report provided by our expert geneticists. The report will not only confirm the presence of SCA10 but also offer insights into the specific mutation, aiding in the understanding of the condition and guiding future medical management.
For more information about the ANO10 gene spinocerebellar ataxia type 10 autosomal recessive genetic test and to schedule your test, please visit DNA Labs UAE.
Early diagnosis and understanding of the genetic basis of SCA10 are essential steps towards managing this challenging condition. With the support of DNA Labs UAE, individuals at risk or showing symptoms of SCA10 can access the critical information needed to make informed health decisions and pursue appropriate treatment options.
