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GPC3 Gene Simpson-Golabi-Behmel Syndrome Type 1 Genetic Test Cost

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

-21%

The GPC3 gene test for Simpson-Golabi-Behmel Syndrome Type 1 is a specialized genetic screening offered by DNA Labs UAE. This test is designed to identify mutations in the GPC3 gene, which are linked to the development of Simpson-Golabi-Behmel Syndrome Type 1 (SGBS1), a rare genetic disorder characterized by pre- and postnatal overgrowth, distinctive facial features, and a variety of organ abnormalities. The condition is primarily seen in males and can have variable expressivity. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations associated with SGBS1.

The cost of the GPC3 gene test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results. Conducting the test at DNA Labs UAE ensures that patients receive accurate and reliable results, as the lab is equipped with state-of-the-art genetic testing technology and staffed by professionals with expertise in genetic disorders. This test is crucial for families seeking a diagnosis for symptoms consistent with Simpson-Golabi-Behmel Syndrome Type 1, as it provides essential information for managing the condition and understanding the risk of recurrence in future pregnancies.

Home  Sample collection service available

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  • This test is not intended for medical diagnosis or treatment
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GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test

Welcome to DNA Labs UAE, your trusted genetic testing laboratory in the UAE. We offer the GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test at a cost of AED 4400.0.

Test Details

The GPC3 gene is associated with Simpson-Golabi-Behmel syndrome type 1 (SGBS1), a rare genetic disorder characterized by overgrowth, distinctive facial features, and multiple congenital anomalies. Our NGS (Next-Generation Sequencing) technology allows us to analyze the DNA sequence of an individual’s genes and identify mutations or variations in the GPC3 gene that may be causing the syndrome.

Test 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: Neurological Disorders
  • Doctor: Neurologist
  • Test Department: Genetics

Pre Test Information

Prior to the GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session will be conducted to draw a pedigree chart of family members affected with GPC3 Gene Simpson-Golabi-Behmel syndrome type 1.

Benefits of the GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test

By analyzing the DNA sequence using NGS, we can provide valuable information about the specific genetic changes present in an individual, allowing for a more accurate diagnosis of SGBS1. This information can also be useful for genetic counseling and family planning purposes.

At DNA Labs UAE, we are committed to providing reliable and accurate genetic testing services. Contact us today to schedule your GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test.

Test Name GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GPC3 Gene Simpson-Golabi-Behmel syndrome type 1 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GPC3 Gene Simpson-Golabi-Behmel syndrome type 1
Test Details

The GPC3 gene is associated with Simpson-Golabi-Behmel syndrome type 1 (SGBS1), a rare genetic disorder characterized by overgrowth, distinctive facial features, and multiple congenital anomalies.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the case of SGBS1, NGS can be used to identify mutations or variations in the GPC3 gene that may be causing the syndrome.

By analyzing the DNA sequence, NGS can provide valuable information about the specific genetic changes present in an individual, allowing for a more accurate diagnosis of SGBS1. This information can also be useful for genetic counseling and family planning purposes.

SKU: TEST-1974 Category:

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