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SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test

4,400 د.إ

-21%

The SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the SNX14 gene, which are known to cause cerebellar ataxia. Cerebellar ataxia is a neurological disorder that affects coordination and balance, often leading to significant impairment in movement and motor functions. The SNX14 gene plays a crucial role in the proper functioning of the cerebellum, and mutations in this gene can disrupt its activity, leading to the symptoms associated with cerebellar ataxia.

This genetic test is particularly important for individuals who exhibit symptoms of cerebellar ataxia or have a family history of the condition, as it can provide a definitive diagnosis. Early detection through this genetic testing can facilitate timely intervention and management of the disorder, potentially improving the quality of life for those affected.

The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any mutations in the SNX14 gene. The procedure is highly accurate and provides valuable genetic insights that can aid in the diagnosis and management of cerebellar ataxia.

At DNA Labs UAE, the cost of the SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test is set at 4400 AED. While the cost may seem substantial, the test offers critical information for affected individuals and their families, guiding treatment decisions and offering a clearer understanding of the genetic underpinnings of their condition.

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SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test

At DNA Labs UAE, we offer the SNX14 gene cerebellar ataxia SNX14 related genetic test to help diagnose individuals with cerebellar ataxia and determine if their condition is caused by mutations in the SNX14 gene. Cerebellar ataxia is a neurological disorder that affects the cerebellum, the part of the brain that controls movement and coordination.

Test Details

The SNX14 gene cerebellar ataxia SNX14 related NGS genetic test is a genetic test that looks for mutations in the SNX14 gene. Mutations in this gene have been associated with autosomal recessive cerebellar ataxia, a form of cerebellar ataxia that is inherited in an autosomal recessive manner.

This test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the SNX14 gene and identify any mutations or variations that may be present. It can help diagnose individuals with cerebellar ataxia and determine if their condition is caused by mutations in the SNX14 gene.

Test Components and Price

The SNX14 gene cerebellar ataxia SNX14 related genetic test costs 4400.0 AED. The test requires a blood sample or extracted DNA, or one drop of blood on an FTA card. The report delivery time is 3 to 4 weeks.

Symptoms and Diagnosis

Cerebellar ataxia is characterized by symptoms such as unsteady gait, lack of coordination, and difficulty with fine motor skills. Diagnosis of cerebellar ataxia involves a clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with SNX14 gene cerebellar ataxia SNX14 related.

Doctor and Test Department

The SNX14 gene cerebellar ataxia SNX14 related genetic test is performed by a neurologist in the Genetics department.

Importance of Genetic Testing

Genetic testing for SNX14 gene cerebellar ataxia can also be helpful for family members of individuals with the condition. It can identify carriers of the mutated gene who may be at risk of passing it on to their children. This information can help families make informed decisions about family planning and genetic counseling.

Test Name SNX14 Gene Cerebellar ataxia SNX14 related Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SNX14 Gene Cerebellar ataxia, SNX14 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SNX14 Gene Cerebellar ataxia, SNX14 related
Test Details

SNX14 gene cerebellar ataxia, SNX14 related NGS genetic test is a genetic test that looks for mutations in the SNX14 gene that can cause cerebellar ataxia. Cerebellar ataxia is a neurological disorder that affects the cerebellum, the part of the brain that controls movement and coordination.

Mutations in the SNX14 gene have been associated with autosomal recessive cerebellar ataxia, a form of cerebellar ataxia that is inherited in an autosomal recessive manner. Autosomal recessive means that an individual must inherit two copies of the mutated gene (one from each parent) to develop the condition.

The SNX14 related NGS genetic test uses next-generation sequencing (NGS) technology to analyze the DNA sequence of the SNX14 gene and identify any mutations or variations that may be present. This test can help diagnose individuals with cerebellar ataxia and determine if their condition is caused by mutations in the SNX14 gene.

Genetic testing can also be helpful for family members of individuals with SNX14 gene cerebellar ataxia, as it can identify carriers of the mutated gene who may be at risk of passing it on to their children. This information can help families make informed decisions about family planning and genetic counseling.