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TCOF1 Gene Treacher Collins Syndrome Type 1 Genetic Test Cost

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

-21%

The TCOF1 gene test for Treacher Collins Syndrome Type 1 is a specialized genetic analysis designed to detect mutations in the TCOF1 gene, which is closely associated with Treacher Collins Syndrome (TCS). TCS is a genetic disorder characterized by distinctive facial anomalies and deformities of the ears, eyes, cheekbones, and chin. This condition is inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the gene can cause the disorder.

Conducted at DNA Labs UAE, this genetic test is crucial for early diagnosis, which can significantly aid in the management and treatment planning for affected individuals. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the TCOF1 gene.

The cost of the TCOF1 gene test for Treacher Collins Syndrome Type 1 at DNA Labs UAE is 4400 AED. This cost covers the comprehensive analysis required to identify the genetic mutation responsible for the syndrome. Early diagnosis through this test can provide families with valuable information regarding the course of the syndrome, potential treatments, and the risk of passing the condition on to future generations.

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TCOF1 Gene Treacher Collins Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the TCOF1 Gene Treacher Collins Syndrome Type 1 Genetic Test at a cost of AED 4400.0. This test is used to diagnose and identify the TCOF1 gene mutations or variations associated with Treacher Collins Syndrome Type 1, also known as mandibulofacial dysostosis.

Test Details

Treacher Collins Syndrome Type 1 is a genetic disorder that affects the development of bones and other tissues in the face. Our NGS (Next Generation Sequencing) genetic testing method allows us to analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup.

Components

  • Price: AED 4400.0
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the TCOF1 Gene Treacher Collins Syndrome Type 1 NGS Genetic DNA 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 by the TCOF1 gene. This information is crucial for accurate diagnosis and genetic counseling.

By identifying mutations or variations in the TCOF1 gene, our genetic test can confirm a diagnosis of Treacher Collins Syndrome Type 1 and provide valuable genetic counseling for affected individuals and their families.

Test Name TCOF1 Gene Treacher Collins syndrome type 1 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TCOF1 Gene Treacher Collins syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TCOF1 Gene Treacher Collins syndrome type 1 NGS Genetic DNA Test gene TCOF1
Test Details

The TCOF1 gene is associated with Treacher Collins syndrome type 1, also known as mandibulofacial dysostosis. This genetic disorder affects the development of bones and other tissues in the face.

NGS (Next Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive view of an individual’s genetic makeup. In the case of Treacher Collins syndrome type 1, NGS genetic testing can be used to identify mutations or variations in the TCOF1 gene that may be responsible for the condition. This can help in confirming a diagnosis and providing genetic counseling for affected individuals and their families.