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SHOC2 Gene Noonan Syndrome-like Genetic Test Cost

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

-21%

The “SHOC2 Gene Noonan Syndrome-like Genetic Test” is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the SHOC2 gene that are associated with a Noonan syndrome-like disorder. This condition shares many characteristics with Noonan syndrome, including distinctive facial features, heart defects, developmental delays, and short stature, but it is caused by specific mutations in the SHOC2 gene. The test involves analyzing the patient’s DNA to identify any abnormalities in the SHOC2 gene that might indicate the presence of the syndrome. With a cost of 4400 AED, this genetic test is a valuable resource for families seeking answers to complex genetic questions, offering them a clearer understanding of their genetic health and enabling healthcare providers to tailor more effective treatment and management plans for affected individuals.

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SHOC2 Gene Noonan Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic lab offering a comprehensive range of genetic tests. In this blog, we will discuss the SHOC2 Gene Noonan Syndrome Genetic Test, its components, cost, symptoms, diagnosis, and more.

Test Details

The SHOC2 gene is associated with Noonan syndrome, a genetic disorder characterized by distinctive facial features, short stature, heart defects, and developmental delays. Our advanced Next-Generation Sequencing (NGS) technology allows us to analyze the SHOC2 gene and identify any mutations or variations that may be present.

Test Components

  • Test Name: SHOC2 Gene Noonan Syndrome Genetic Test
  • 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

Prior to the SHOC2 Gene Noonan Syndrome Genetic Test, it is important to provide the clinical history of the patient who is going for the test. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with SHOC2 Gene Noonan Syndrome Genetic Test gene SHOC2.

Diagnosis and Benefits

NGS genetic testing is a high-throughput method that allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. In the context of Noonan syndrome, NGS testing can help confirm a diagnosis by identifying specific mutations in the SHOC2 gene.

This test can also be used to assess the genetic risk for other family members or provide genetic counseling for couples planning to have children. It provides valuable information for diagnosing Noonan syndrome and guiding appropriate medical management and genetic counseling.

At DNA Labs UAE, we are committed to providing accurate and reliable genetic testing services. Our SHOC2 Gene Noonan Syndrome Genetic Test can help in early diagnosis and effective management of Noonan syndrome.

For more information or to schedule a test, please contact us.

Test Name SHOC2 Gene Noonan syndrom like 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 SHOC2 Gene Noonan syndrom like NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SHOC2 Gene Noonan syndrom like NGS Genetic DNA Test gene SHOC2
Test Details

The SHOC2 gene is associated with Noonan syndrome, which is a genetic disorder characterized by distinctive facial features, short stature, heart defects, and developmental delays. Next-generation sequencing (NGS) genetic testing can be used to analyze the SHOC2 gene and identify any mutations or variations that may be present.

NGS genetic testing is a high-throughput method that allows for the simultaneous analysis of multiple genes, providing a comprehensive view of an individual’s genetic makeup. This type of testing can detect various types of genetic alterations, including single nucleotide variants, small insertions or deletions, and larger structural changes.

In the context of Noonan syndrome, NGS testing can help confirm a diagnosis by identifying specific mutations in the SHOC2 gene. It can also be used to assess the genetic risk for other family members or provide genetic counseling for couples planning to have children.

Overall, NGS genetic testing for the SHOC2 gene can provide valuable information for diagnosing Noonan syndrome and guiding appropriate medical management and genetic counseling.

SKU: TEST-4276 Category:

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