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CTC1 Gene Coat Plus Syndrome Genetic Test

4,400 د.إ

-21%

The “CTC1 Gene Coat Plus Syndrome Genetic Test” is a specialized genetic screening designed to identify mutations in the CTC1 gene, which is closely associated with Coat Plus Syndrome. This syndrome is a rare genetic disorder characterized by a variety of symptoms including retinal dystrophy, intracranial calcifications, bone marrow failure, and others. The test plays a crucial role in the early diagnosis and management of the condition, allowing healthcare professionals to tailor treatments and interventions to the specific needs of the patient.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, this test is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring accurate and reliable results. By opting for this test, patients and their families can gain invaluable insights into their genetic makeup, paving the way for informed healthcare decisions and personalized medical care.

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  • 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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CTC1 Gene Coat plus syndrome Genetic Test

At DNA Labs UAE, we offer the CTC1 Gene Coat plus syndrome Genetic Test. This test is designed to diagnose the rare genetic disorder known as Coat plus syndrome, which affects multiple systems in the body including the skin, hair, eyes, and nervous system.

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: Ophthalmology Disorders
  • Doctor: Ophthalmologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the CTC1 Gene Coat plus syndrome Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected with CTC1 Gene Coat plus syndrome NGS Genetic DNA Test gene CTC1.

Test Details

Coat plus syndrome is a rare genetic disorder that is caused by mutations in the CTC1 gene. This gene provides instructions for making a protein called CTC1, which is involved in maintaining the ends of chromosomes known as telomeres. Telomeres protect the genetic material inside cells from damage.

The CTC1 Gene Coat plus syndrome Genetic Test utilizes NGS technology to sequence the CTC1 gene and identify any mutations that may be present. This test can confirm a diagnosis of Coat plus syndrome and provide information about the specific genetic changes causing the condition. It can also identify carriers of the mutation in families with a history of the disorder.

Next-generation sequencing (NGS) is a powerful technology that allows for the rapid and accurate sequencing of large amounts of genetic material. It has revolutionized the field of genetics and is widely used in clinical practice for the diagnosis and management of genetic disorders.

For more information about the CTC1 Gene Coat plus syndrome Genetic Test or to schedule an appointment, please contact DNA Labs UAE.

Test Name CTC1 Gene Coat plus 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 Ophthalmology Disorders
Doctor Ophthalmologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for CTC1 Gene Coat plus syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with CTC1 Gene Coat plus syndrome NGS Genetic DNA Test gene CTC1
Test Details

Coat plus syndrome is a rare genetic disorder that affects multiple systems in the body, including the skin, hair, eyes, and nervous system. It is caused by mutations in the CTC1 gene, which provides instructions for making a protein called CTC1. This protein is involved in maintaining the ends of chromosomes, known as telomeres, which protect the genetic material inside cells from damage.

A NGS genetic test for Coat plus syndrome would involve sequencing the CTC1 gene to identify any mutations that may be present. This test can help confirm a diagnosis of Coat plus syndrome and provide information about the specific genetic changes that are causing the condition. It may also be used to identify carriers of the mutation in families with a history of the disorder.

NGS, or next-generation sequencing, is a powerful technology that allows for the rapid and accurate sequencing of large amounts of genetic material. It has revolutionized the field of genetics and is now widely used in clinical practice for the diagnosis and management of genetic disorders.