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COL11A1 Gene Marshall Syndrome Genetic Test Cost

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

-21%

The COL11A1 Gene Marshall Syndrome Genetic Test is a specific diagnostic tool used to identify mutations in the COL11A1 gene, which is known to be associated with Marshall Syndrome. Marshall Syndrome is a rare genetic disorder characterized by a spectrum of symptoms including distinctive facial features, eye abnormalities, hearing loss, and skeletal anomalies. The test plays a crucial role in the early detection and management of the condition, enabling healthcare providers to offer personalized treatment plans and genetic counseling for affected individuals and their families.

Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, this test ensures high accuracy and reliability. The test cost is set at 4400 AED, reflecting the comprehensive nature of the genetic analysis and the specialized expertise required to interpret the results. By choosing DNA Labs UAE for the COL11A1 Gene Marshall Syndrome Genetic Test, patients can expect state-of-the-art services, confidentiality, and support throughout the testing process.

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
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COL11A1 Gene Marshall Syndrome Genetic Test

At DNA Labs UAE, we offer the COL11A1 Gene Marshall Syndrome Genetic Test at a cost of AED 4400.0.

Test Components:

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

Report Delivery:

Results will be delivered within 3 to 4 weeks.

Method:

The test is conducted using NGS (Next-Generation Sequencing) technology.

Test Type:

This test focuses on Ear Nose Throat Disorders and is recommended for patients referred by an ENT Doctor.

Test Department:

The test is conducted by our Genetics department.

Pre Test Information:

Prior to the test, it is important to provide the clinical history of the patient who is going for the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with the PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN36.

Test Details:

The COL11A1 gene is associated with Marshall syndrome, also known as type II Stickler syndrome. Marshall syndrome is a rare genetic disorder characterized by abnormalities in the connective tissues, affecting various parts of the body including the eyes, ears, and skeleton.

NGS genetic testing is a technique used to analyze multiple genes simultaneously and detect mutations or variations in the DNA sequence. In the context of Marshall syndrome, NGS genetic testing can identify mutations or variations in the COL11A1 gene that may be responsible for the development of the disorder.

By analyzing the entire coding region of the COL11A1 gene, NGS testing provides a comprehensive assessment of genetic changes associated with Marshall syndrome. This information can confirm a diagnosis, predict the risk of developing the condition, and inform treatment decisions.

It is important to note that genetic testing for Marshall syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.

Test Name COL11A1 Gene Marshall syndrome Genetic 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 Ear Nose Throat Disorders
Doctor ENT Doctor
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN23 Gene Ciliogenesis related disorder NGS Genetic DNA Test gene PTPN36
Test Details

COL11A1 gene is associated with Marshall syndrome, also known as type II Stickler syndrome. Marshall syndrome is a rare genetic disorder characterized by abnormalities in the connective tissues, which can affect various parts of the body including the eyes, ears, and skeleton.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously and detect mutations or variations in the DNA sequence. In the context of Marshall syndrome, NGS genetic testing can be used to identify mutations or variations in the COL11A1 gene that may be responsible for the development of the disorder.

By analyzing the entire coding region of the COL11A1 gene, NGS testing can provide a comprehensive assessment of genetic changes that may be associated with Marshall syndrome. This can help in confirming a diagnosis, predicting the risk of developing the condition, and informing treatment decisions.

It is important to note that genetic testing for Marshall syndrome should be performed by a qualified healthcare professional or genetic counselor who can interpret the results and provide appropriate counseling and guidance.

SKU: TEST-2759 Category:

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