LARS2 Gene Perrault Syndrome Type 4 Genetic Test sale cost 4400 AED
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LARS2 Gene Perrault Syndrome Type 4 Genetic Test Cost

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

-21%

The LARS2 gene Perrault Syndrome Type 4 genetic test is a specialized diagnostic tool used to detect mutations in the LARS2 gene, which are linked to Perrault Syndrome Type 4. Perrault Syndrome is a rare genetic disorder characterized by sensorineural hearing loss in both males and females and premature ovarian failure in females. The LARS2 gene plays a crucial role in mitochondrial function, and mutations in this gene can disrupt normal cellular activities, leading to the symptoms observed in affected individuals.

This genetic test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to identify any mutations in the LARS2 gene. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the comprehensive insights it provides.

Opting for this test can be particularly important for families with a history of Perrault Syndrome or individuals showing symptoms related to the disorder. Early diagnosis through genetic testing can aid in better understanding the condition, facilitating informed decisions about management and treatment options. It also helps in genetic counseling for affected families, providing them with crucial information regarding the inheritance patterns and risks of passing the condition to future generations.

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LARS2 Gene Perrault syndrome type 4 Genetic Test

At DNA Labs UAE, we offer the LARS2 Gene Perrault syndrome type 4 Genetic Test for individuals who may be affected by this rare genetic disorder. This test is designed to analyze the LARS2 gene, which is associated with Perrault syndrome type 4.

Test Components

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 LARS2 Gene Perrault syndrome type 4 NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by Perrault syndrome type 4.

Test Details

Perrault syndrome type 4 is a rare genetic disorder characterized by sensorineural hearing loss in both males and females, as well as ovarian dysfunction in females. The LARS2 gene is associated with this syndrome. NGS genetic testing is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes. In the context of Perrault syndrome type 4, NGS genetic testing can identify potential genetic variants or mutations in the LARS2 gene, aiding in diagnosis confirmation and genetic counseling for affected individuals and their families.

Test Name LARS2 Gene Perrault syndrome type 4 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 LARS2 Gene Perrault syndrome type 4 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with LARS2 Gene Perrault syndrome type 4
Test Details

The LARS2 gene is associated with Perrault syndrome type 4, which is a rare genetic disorder characterized by sensorineural hearing loss in both males and females, as well as ovarian dysfunction in females.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. In the context of Perrault syndrome type 4, NGS genetic testing can be used to analyze the LARS2 gene to identify any potential genetic variants or mutations that may be causing the disorder. This can help in confirming a diagnosis and providing genetic counseling to affected individuals and their families.

SKU: TEST-1912