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TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test Cost

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

-21%

The “TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Genetic Test” is a specialized diagnostic tool used to identify mutations in the TMCO1 gene, which have been associated with a rare genetic disorder. This condition is characterized by distinctive craniofacial features, skeletal abnormalities, and intellectual disability. The test is crucial for the accurate diagnosis of the syndrome, enabling healthcare providers to develop a personalized treatment and management plan for affected individuals.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test involves analyzing the patient’s DNA to look for specific mutations in the TMCO1 gene that are linked to the syndrome. The process is comprehensive, ensuring a high degree of accuracy in the diagnosis of this complex condition.

The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to conduct this advanced genetic analysis. For families and individuals facing the possibility of this rare syndrome, the test offers valuable insights, guiding medical and support strategies to improve quality of life and manage the syndrome’s various challenges.

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  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test

Are you concerned about craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome? DNA Labs UAE offers the TMCO1 Gene Genetic Test to help diagnose and understand this syndrome. Read on to learn more about the test details, components, price, and more.

Test Components and Price

The TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation Syndrome Genetic Test is priced at 4400.0 AED. The test components include:

  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Method: NGS Technology
  • Test Type: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the TMCO1 Gene Craniofacial Dysmorphism Skeletal Anomalies and Mental Retardation 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 by the syndrome. This will help in understanding the genetic basis of the syndrome and guide the testing process.

Test Details

The TMCO1 gene is associated with a syndrome characterized by craniofacial dysmorphism, skeletal anomalies, and mental retardation. NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes or even the entire genome simultaneously. In the case of the TMCO1 gene syndrome, NGS genetic testing can identify mutations or variations in the TMCO1 gene that may be responsible for the syndrome.

By sequencing the DNA of an individual, NGS technology can detect changes in the TMCO1 gene associated with craniofacial dysmorphism, skeletal anomalies, and mental retardation. This information is crucial for diagnosing the syndrome, understanding its genetic basis, and potentially providing treatment or management strategies.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors. They can provide appropriate guidance and support to individuals and families undergoing genetic testing.

Test Name TMCO1 Gene Craniofacial dysmorphism skeletal anomalies and mental retardation 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with TMCO1 Gene Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome NGS Genetic DNA Test gene TMCO1
Test Details

The TMCO1 gene is associated with a syndrome characterized by craniofacial dysmorphism (abnormal facial features), skeletal anomalies (abnormalities in the bones), and mental retardation (intellectual disability).

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the simultaneous analysis of multiple genes or even the entire genome. In the context of TMCO1 gene syndrome, NGS genetic testing can be used to identify mutations or variations in the TMCO1 gene that may be responsible for the syndrome.

By sequencing the DNA of an individual, NGS technology can detect changes in the TMCO1 gene that may be associated with craniofacial dysmorphism, skeletal anomalies, and mental retardation. This information can be helpful for diagnosing the syndrome, understanding its genetic basis, and potentially providing information for treatment or management strategies.

It is important to note that genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support to individuals and families undergoing genetic testing.