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GPC6 Gene Omodysplasia Type 1 Genetic Test Cost

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

-21%

The GPC6 gene omodysplasia type 1 genetic test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the GPC6 gene, which are associated with omodysplasia type 1, a rare genetic disorder. This condition is characterized by skeletal abnormalities, including short stature, short limbs, and facial dysmorphisms. The test is crucial for early diagnosis, allowing for appropriate management and intervention strategies to be implemented for affected individuals.

Priced at 4400 AED, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic mutations in the GPC6 gene. The results can provide valuable information for families regarding the genetic basis of the condition, risk of recurrence in future pregnancies, and potential treatment pathways. Conducted at the state-of-the-art facilities of DNA Labs UAE, this genetic test represents a critical step towards personalized medicine for patients with omodysplasia type 1, offering hope and support to affected families.

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  • This test is not intended for medical diagnosis or treatment
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GPC6 Gene Omodysplasia Type 1 Genetic Test

Welcome to DNA Labs UAE, where we offer the GPC6 Gene Omodysplasia Type 1 Genetic Test. This test is designed to identify mutations or variations in the GPC6 gene, which is associated with a genetic disorder called omodysplasia type 1.

Test Components and Price

  • Test Name: GPC6 Gene Omodysplasia Type 1 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: Osteology Dermatology Immunology Disorders
  • Doctor: Dermatologist
  • Test Department: Genetics

Pre Test Information

Before undergoing the GPC6 Gene Omodysplasia Type 1 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected by the GPC6 Gene Omodysplasia Type 1 Genetic Test gene GPC6.

Test Details

The GPC6 gene is associated with omodysplasia type 1, a genetic disorder characterized by skeletal abnormalities such as short stature, abnormal bone development, and joint deformities. The NGS genetic testing method is used to analyze the DNA sequence of an individual’s genes and identify specific genetic variations or mutations related to a particular disorder or condition.

In the case of omodysplasia type 1, the GPC6 gene is analyzed using NGS genetic testing to identify any mutations or variations that may be causing the disorder. A DNA sample is obtained from the individual, typically through a blood or saliva sample, and then sequenced using advanced technology. The results of the test can help diagnose omodysplasia type 1 and provide information for genetic counseling and management of the condition.

It is important to note that genetic testing for omodysplasia type 1 is usually recommended for individuals who have symptoms or a family history of the disorder. The test should be ordered and interpreted by a healthcare professional or genetic counselor with expertise in genetic testing and rare genetic disorders.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. Contact us today to learn more about the GPC6 Gene Omodysplasia Type 1 Genetic Test and how it can help you and your family.

Test Name GPC6 Gene Omodysplasia 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 Osteology Dermatology Immunology Disorders
Doctor Dermatologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for GPC6 Gene Omodysplasia type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GPC6 Gene Omodysplasia type 1 NGS Genetic DNA Test gene GPC6
Test Details

The GPC6 gene is associated with a genetic disorder called omodysplasia type 1. This disorder is characterized by skeletal abnormalities, including short stature, abnormal bone development, and joint deformities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It can identify specific genetic variations or mutations that may be associated with a particular disorder or condition. In the case of omodysplasia type 1, NGS genetic testing can be used to analyze the GPC6 gene for any mutations or variations that may be causing the disorder.

The NGS genetic test for GPC6 gene omodysplasia type 1 involves obtaining a DNA sample from the individual, typically through a blood or saliva sample. The DNA is then sequenced using advanced technology to identify any variations or mutations in the GPC6 gene. The results of the test can help diagnose omodysplasia type 1 and provide information for genetic counseling and management of the condition.

It’s important to note that genetic testing for omodysplasia type 1 is typically only recommended for individuals who have symptoms or a family history of the disorder. The test should be ordered and interpreted by a healthcare professional or genetic counselor with expertise in genetic testing and rare genetic disorders.