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PTPN11 Gene Noonan Syndrome Type 1 Genetic Test Cost

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

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The PTPN11 gene Noonan Syndrome Type 1 genetic test is a specialized diagnostic tool used to identify mutations in the PTPN11 gene, which are linked to Noonan Syndrome Type 1. Noonan Syndrome is a genetic disorder that affects various parts of the body and is characterized by distinctive facial features, heart defects, developmental delays, and other physical abnormalities. The PTPN11 gene plays a crucial role in the development and function of many body systems, and mutations in this gene are the most common genetic cause of Noonan Syndrome.

This test is particularly important for individuals who exhibit symptoms of Noonan Syndrome or have a family history of the condition, as it can provide a definitive diagnosis. Early diagnosis is vital for managing the symptoms and improving the quality of life for those affected. The test involves analyzing the DNA to look for specific mutations in the PTPN11 gene that are known to cause Noonan Syndrome.

The PTPN11 gene Noonan Syndrome Type 1 genetic test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable test results. By opting for this test at DNA Labs UAE, individuals can take an important step towards understanding their genetic health and making informed decisions about their care and the care of their families.

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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PTPN11 Gene Noonan Syndrome Type 1 Genetic Test

At DNA Labs UAE, we offer the PTPN11 Gene Noonan Syndrome Type 1 Genetic Test. This test helps in diagnosing and understanding Noonan syndrome type 1, a genetic disorder characterized by distinctive facial features, short stature, heart defects, and developmental delays.

Test Components and Price

The PTPN11 Gene Noonan Syndrome Type 1 Genetic Test is priced at AED 4400.0. 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the PTPN11 Gene Noonan Syndrome Type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session is conducted to draw a pedigree chart of family members affected by the PTPN11 gene. This information helps in better understanding the genetic composition of the family and aids in accurate diagnosis.

Test Details

The PTPN11 gene is associated with Noonan syndrome type 1. To detect mutations or variations in this gene, we utilize NGS (Next-Generation Sequencing) technology. NGS allows for the simultaneous analysis of multiple genes, including the PTPN11 gene.

During the test, a DNA sample is collected from the individual being tested. This sample can be obtained through a blood or saliva sample. The collected DNA is then sequenced using NGS technology to identify any variations or mutations in the PTPN11 gene.

The results of the NGS genetic test help confirm a diagnosis of Noonan syndrome type 1 and provide information about the specific genetic variant involved. This information is crucial for determining the most appropriate course of treatment and management for individuals with Noonan syndrome type 1.

Test Name PTPN11 Gene Noonan 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 PTPN11 Gene Noonan syndrome type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with PTPN11 Gene Noonan syndrome type 1 NGS Genetic DNA Test gene PTPN11
Test Details

The PTPN11 gene is associated with Noonan syndrome type 1, a genetic disorder characterized by distinctive facial features, short stature, heart defects, and developmental delays.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the simultaneous analysis of multiple genes, including the PTPN11 gene. It can detect mutations or variations in the PTPN11 gene that may be responsible for causing Noonan syndrome type 1.

The NGS genetic test for Noonan syndrome type 1 involves collecting a DNA sample, typically through a blood or saliva sample, from the individual being tested. The DNA is then sequenced using NGS technology to identify any variations or mutations in the PTPN11 gene.

The results of the NGS genetic test can help confirm a diagnosis of Noonan syndrome type 1 and provide information about the specific genetic variant involved. This information can be useful for determining the best course of treatment and management for individuals with Noonan syndrome type 1.

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