ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test sale cost 4400 AED
REEP2 Gene SPG72 Genetic Test sale cost 4400 AED REEP2 Gene SPG72 Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
ATXN3 Gene Spinocerebellar Ataxia Type 3 Autosomal Dominant Genetic Test sale cost 4400 AED ATXN3 Gene Spinocerebellar Ataxia Type 3 Autosomal Dominant Genetic Test Cost 5,600 د.إ Original price was: 5,600 د.إ.4,400 د.إCurrent price is: 4,400 د.إ.
Sale!

ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test Cost

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

-21%

The ITPR1 gene plays a crucial role in the proper functioning of the cerebellum, a part of the brain responsible for coordinating movement. Mutations in this gene can lead to Spinocerebellar Ataxia Type 15 (SCA15), a genetic disorder characterized by progressive deterioration of motor skills, balance issues, and coordination difficulties. The ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test is a specialized diagnostic tool designed to detect mutations in the ITPR1 gene, confirming the diagnosis of SCA15. This test is particularly valuable for individuals showing symptoms of ataxia or those with a family history of the condition, as it can provide definitive genetic evidence of SCA15.

Conducted by DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the ITPR1 gene. The cost of the test is set at 4400 AED, reflecting the intricate technology and expertise required to accurately identify mutations associated with the condition. By opting for this test, patients and their families can gain crucial insights into their genetic makeup, enabling informed decisions about management and treatment options for Spinocerebellar Ataxia Type 15.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
Guaranteed Safe Checkout

ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test

At DNA Labs UAE, we offer the ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test. This test is designed to diagnose and provide information about the rare genetic disorder known as Spinocerebellar Ataxia Type 15 (SCA15). SCA15 is characterized by the progressive degeneration of the cerebellum, resulting in uncoordinated movements, balance problems, and other neurological symptoms.

Test Details

The ITPR1 gene is associated with SCA15, and mutations in this gene can cause the condition. Our genetic testing method, NGS (Next-Generation Sequencing) technology, allows for the analysis of multiple genes simultaneously. With NGS genetic testing, we can identify mutations or variations in the ITPR1 gene that may be responsible for the development of SCA15.

Test Components and Price

The ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test is priced at AED 4400.0. The test requires a blood or extracted DNA sample, or one drop of blood on an FTA card. The report will be delivered within 3 to 4 weeks.

Test Type and Doctor

This test falls under the category of Neurological Disorders. It is recommended to consult a Neurologist for this test.

Test Department

The ITPR1 Gene Spinocerebellar Ataxia Type 15 Genetic Test is conducted in our Genetics department.

Pre Test Information

Prior to taking the test, it is important to provide the clinical history of the patient who is undergoing the ITPR1 Gene Spinocerebellar Ataxia Type 15 NGS Genetic DNA Test. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected by SCA15.

Benefits of Genetic Testing for SCA15

Genetic testing for SCA15 can provide a definitive diagnosis and help guide treatment and management strategies. It can be beneficial for individuals who have symptoms of the disorder or have a family history of SCA15. Additionally, genetic testing can be used for carrier testing or prenatal testing for individuals who may be at risk of passing on the mutated gene to their children.

Important Considerations

It is crucial to undergo genetic testing for SCA15 under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.

Test Name ITPR1 Gene Spinocerebellar ataxia type 15 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 ITPR1 Gene Spinocerebellar ataxia type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with ITPR1 Gene Spinocerebellar ataxia type 15
Test Details

Spinocerebellar ataxia type 15 (SCA15) is a rare genetic disorder characterized by progressive degeneration of the cerebellum, leading to uncoordinated movements, balance problems, and other neurological symptoms. The ITPR1 gene is associated with SCA15, and mutations in this gene can cause the condition.

NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the analysis of multiple genes simultaneously. In the case of SCA15, NGS genetic testing can be used to identify mutations or variations in the ITPR1 gene that may be responsible for the development of the disorder.

NGS testing involves obtaining a DNA sample, typically through a blood or saliva sample, and then sequencing the DNA to identify any genetic variations or mutations. This can help to diagnose SCA15 and provide information about the specific genetic variant that is causing the condition.

Genetic testing for SCA15 can be helpful for individuals who have symptoms of the disorder or have a family history of SCA15. It can provide a definitive diagnosis and help guide treatment and management strategies. Additionally, genetic testing can also be used for carrier testing or prenatal testing for individuals who may be at risk of passing on the mutated gene to their children.

It is important to note that genetic testing for SCA15 should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and support throughout the testing process.

SKU: TEST-2059