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TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test Cost

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

-21%

The TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test is a specialized diagnostic tool designed to identify mutations in the TSEN34 gene, which are linked to Pontocerebellar Hypoplasia Type 2C (PCH2C). PCH2C is a rare genetic disorder characterized by the underdevelopment of the cerebellum and pons, two critical regions of the brain responsible for controlling movement and coordination. This condition manifests early in life and can lead to significant neurological impairments, including difficulties with movement, speech, and in some cases, intellectual disabilities.

The test is conducted by DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. Utilizing advanced genomic sequencing technologies, DNA Labs UAE offers this test at a cost of 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in their state-of-the-art laboratory facilities. The aim is to detect any mutations in the TSEN34 gene that may indicate the presence of PCH2C, thereby providing crucial information for diagnosis, management, and familial genetic counseling.

Given the complexity and rarity of Pontocerebellar Hypoplasia Type 2C, the TSEN34 Gene Test is an invaluable resource for affected families seeking answers and medical professionals aiming to tailor care plans to the specific needs of their patients.

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  • This test is not intended for medical diagnosis or treatment
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TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test

At DNA Labs UAE, we offer the TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test for individuals who may be affected by this rare genetic disorder. Pontocerebellar hypoplasia type 2C (PCH2C) is a condition that affects the development of the brain, specifically the pons and cerebellum, resulting in various neurological symptoms.

The TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test utilizes NGS (Next-Generation Sequencing) technology, which allows for the efficient analysis of multiple genes simultaneously. By analyzing the patient’s DNA sample, this test can identify mutations or variations in the TSEN34 gene that may be responsible for the disorder.

It is important to note that NGS genetic testing for PCH2C may not be widely available and may require specialized testing laboratories or genetic centers. Therefore, it is recommended to consult with a healthcare provider or genetic counselor to determine the availability and appropriateness of this test for a specific individual.

Test Details:

  • Test Name: TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information:

Prior to undergoing the TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic 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 TSEN34 Gene Pontocerebellar Hypoplasia Type 2C. This information will aid in the accurate interpretation of the test results.

Benefits of the Test:

The TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test can provide valuable information for various purposes:

  • Confirming a diagnosis of PCH2C
  • Genetic counseling
  • Family planning
  • Identifying potential future treatment options

If you suspect that you or your loved one may be affected by PCH2C and would like to undergo the TSEN34 Gene Pontocerebellar Hypoplasia Type 2C Genetic Test, please consult with a healthcare provider or genetic counselor for further guidance.

Test Name TSEN34 Gene Pontocerebellar hypoplasia type 2C 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 TSEN34 Gene Pontocerebellar hypoplasia type 2C NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with TSEN34 Gene Pontocerebellar hypoplasia type 2C
Test Details

The TSEN34 gene is associated with a rare genetic disorder called pontocerebellar hypoplasia type 2C (PCH2C). This disorder affects the development of the brain, specifically the pons and cerebellum, leading to various neurological symptoms.

NGS (Next-Generation Sequencing) genetic testing is a type of DNA sequencing technology that allows for the rapid and efficient analysis of multiple genes simultaneously. In the context of PCH2C, NGS genetic testing can be used to identify mutations or variations in the TSEN34 gene that may be responsible for the disorder.

By analyzing the patient’s DNA sample, NGS genetic testing can provide valuable information about the presence of specific mutations in the TSEN34 gene, helping to confirm a diagnosis of PCH2C. This information can also be useful for genetic counseling, family planning, and potential future treatment options.

It’s important to note that NGS genetic testing for PCH2C may not be widely available and may require specialized testing laboratories or genetic centers. A healthcare provider or genetic counselor can provide more information about the availability and appropriateness of this test for a specific individual.

SKU: TEST-1925 Category:

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