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DNAJC3 Gene Ataxia Combined Cerebellar and Peripheral with Hearing Loss and Diabetes Mellitus Genetic Test Cost

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

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The DNAJC3 gene ataxia combined cerebellar and peripheral with hearing loss and diabetes mellitus genetic test is a comprehensive diagnostic tool available at DNA Labs UAE. This specialized test, priced at 4400 AED, is designed to identify mutations in the DNAJC3 gene, which are linked to a rare, inherited disorder. This condition is characterized by a complex spectrum of symptoms including ataxia (a lack of muscle coordination affecting speech, eye movements, and the ability to swallow), peripheral neuropathy, hearing loss, and diabetes mellitus.

By analyzing the DNAJC3 gene, this test can confirm a diagnosis, helping in the management and treatment planning for individuals showing symptoms of this disorder. Early diagnosis through genetic testing is crucial for managing the condition effectively, allowing for tailored treatment strategies that can significantly improve the quality of life for affected individuals. DNA Labs UAE provides this test with a focus on accuracy, confidentiality, and comprehensive support for patients and their families navigating the implications of genetic disorders.

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DNAJC3 Gene Ataxia Genetic Test

At DNA Labs UAE, we offer the DNAJC3 Gene Ataxia combined cerebellar and peripheral with hearing loss and diabetes mellitus Genetic Test. This test helps diagnose and manage a rare neurological disorder known as Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus.

Test Details

The DNAJC3 gene is associated with Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disorder.

NGS genetic testing, which utilizes Next-Generation Sequencing (NGS) technology, can be used to detect mutations in the DNAJC3 gene. This type of testing analyzes multiple genes simultaneously, providing a more comprehensive analysis of an individual’s genetic makeup.

The results of NGS testing can help healthcare providers diagnose and manage this condition, as well as provide genetic counseling to affected individuals and their families.

Test Components and Price

  • Test Name: DNAJC3 Gene Ataxia combined cerebellar and peripheral with hearing loss and diabetes mellitus Genetic Test
  • Price: 4400.0 AED

Sample Condition

The DNAJC3 Gene Ataxia Genetic Test requires either blood, extracted DNA, or one drop of blood on an FTA Card as the sample condition.

Report Delivery

The test results will be delivered within 3 to 4 weeks.

Method

The DNAJC3 Gene Ataxia Genetic Test utilizes NGS technology for analysis.

Test Type

This test is specifically designed for diagnosing neurological disorders.

Doctor

The test is conducted under the supervision of a neurologist.

Test Department

The DNAJC3 Gene Ataxia Genetic Test is conducted in the Genetics department.

Pre Test Information

Before undergoing the DNAJC3 Gene Ataxia Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is recommended to draw a pedigree chart of family members affected with DNAJC3 Gene Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus.

Test Name DNAJC3 Gene Ataxia combined cerebellar and peripheral with hearing loss and diabetes mellitus 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 DNAJC3 Gene Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with DNAJC3 Gene Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus
Test Details

DNAJC3 gene is associated with a rare neurological disorder known as Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disorder.

NGS genetic testing can be used to detect mutations in the DNAJC3 gene. This type of testing analyzes multiple genes simultaneously and can provide a more comprehensive analysis of an individual’s genetic makeup. The results of NGS testing can help healthcare providers diagnose and manage this condition, as well as provide genetic counseling to affected individuals and their families.

SKU: TEST-1072 Category:

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