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KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test is a specialized diagnostic tool designed to identify mutations in the KIF1C gene, which are linked to the development of Spastic Ataxia Type 2, a rare autosomal recessive disorder. This condition is characterized by progressive muscle stiffness (spasticity) and coordination problems (ataxia), affecting an individual’s ability to control muscle movements smoothly and precisely.

Conducted at DNA Labs UAE, a reputable genetic testing facility known for its advanced diagnostic solutions, this test is crucial for early detection and management of the disorder. By analyzing an individual’s DNA sample, typically obtained through a blood draw, the test can pinpoint specific genetic alterations in the KIF1C gene that contribute to the manifestation of Spastic Ataxia Type 2.

The cost of the KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test is set at 4400 AED. Although this price may seem significant, the value of the test lies in its ability to provide essential genetic information. This information not only aids in the accurate diagnosis and understanding of the disorder but also helps in tailoring personalized management plans, potentially improving the quality of life for affected individuals and their families. Early diagnosis through genetic testing can be instrumental in accessing appropriate treatments and support services, making it a valuable investment in the long-term health and well-being of those at risk for or affected by Spastic Ataxia Type 2.

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KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test

Welcome to the DNA Labs UAE blog, where we provide detailed information about genetic testing and disorders. In this blog post, we will discuss the KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test.

Test Name: KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card

Report Delivery: 3 to 4 Weeks

Method: NGS Technology

Test Type: Neurological Disorders

Doctor: Neurologist

Test Department: Genetics

Pre Test Information

Before undergoing the KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with the disorder.

Test Details

The KIF1C gene is associated with a genetic disorder called spastic ataxia type 2, which is inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene (one from each parent) in order to develop the disorder.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify mutations or variations in those genes. In the case of spastic ataxia type 2, NGS genetic testing can be used to identify mutations in the KIF1C gene that may be responsible for the disorder.

By identifying specific mutations in the KIF1C gene, NGS genetic testing can help confirm a diagnosis of spastic ataxia type 2 and provide valuable information for genetic counseling and family planning. It can also assist in determining the prognosis and potential treatment options for affected individuals.

Test Name KIF1C Gene Spastic ataxia type 2 autosomal recessive 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 KIF1C Gene Spastic ataxia type 2, autosomal recessive NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with KIF1C Gene Spastic ataxia type 2, autosomal recessive
Test Details

The KIF1C gene is associated with a genetic disorder called spastic ataxia type 2, which 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) in order to develop the disorder.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously and identify mutations or variations in those genes. In the case of spastic ataxia type 2, NGS genetic testing can be used to identify mutations in the KIF1C gene that may be responsible for the disorder.

By identifying specific mutations in the KIF1C gene, NGS genetic testing can help confirm a diagnosis of spastic ataxia type 2 and provide valuable information for genetic counseling and family planning. It can also assist in determining the prognosis and potential treatment options for affected individuals.

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