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GORAB Gene Geroderma osteodysplasticum Genetic Test Cost

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

-21%

The GORAB Gene Geroderma Osteodysplasticum Genetic Test is a specialized diagnostic tool designed to identify mutations in the GORAB gene, which are linked to Geroderma Osteodysplasticum (GO). GO is a rare genetic disorder characterized by skin laxity, growth retardation, and skeletal abnormalities. This condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.

Conducted at DNA Labs UAE, this test is pivotal for early diagnosis and management of the disorder. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed to detect the presence of specific mutations in the GORAB gene that are known to cause the condition.

The cost of the GORAB Gene Geroderma Osteodysplasticum Genetic Test is set at 4400 AED. While the price may seem steep, the value of this test lies in its ability to provide essential information for the accurate diagnosis and treatment planning for individuals suspected of having this rare condition. Early diagnosis can significantly influence the management and quality of life of the affected individuals, making this test a crucial step for families with a history of Geroderma Osteodysplasticum.

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GORAB Gene Geroderma osteodysplasticum Genetic Test

Welcome to DNA Labs UAE, where we offer the GORAB Gene Geroderma osteodysplasticum Genetic Test. This test is designed to help diagnose and understand the rare genetic disorder called Geroderma Osteodysplasticum (GO).

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

Prior to undergoing the GORAB Gene Geroderma osteodysplasticum NGS Genetic DNA 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 with the GORAB Gene Geroderma osteodysplasticum NGS Genetic DNA Test gene GORAB.

Test Details

The GORAB gene is associated with Geroderma Osteodysplasticum (GO), a rare genetic disorder characterized by a premature aging appearance, skeletal abnormalities, and skin abnormalities. Our NGS (Next-Generation Sequencing) technology allows for the analysis of multiple genes simultaneously, including the GORAB gene. By sequencing the GORAB gene, we can identify any mutations or variations that may be contributing to the development of GO. This test can aid in diagnosis, understanding the underlying cause of the condition, and potentially guiding treatment options.

Test Name GORAB Gene Geroderma osteodysplasticum 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 GORAB Gene Geroderma osteodysplasticum NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GORAB Gene Geroderma osteodysplasticum NGS Genetic DNA Test gene GORAB
Test Details

The GORAB gene is associated with a rare genetic disorder called Geroderma Osteodysplasticum (GO). GO is characterized by a premature aging appearance, skeletal abnormalities, and skin abnormalities.

NGS (Next-Generation Sequencing) is a genetic testing method that allows for the analysis of multiple genes simultaneously. It is used to identify mutations or variations in genes, including the GORAB gene, that may be associated with certain genetic disorders.

In the context of GO, an NGS genetic test would involve sequencing the GORAB gene to identify any mutations or variations that may be contributing to the development of the disorder. This can help with diagnosis, understanding the underlying cause of the condition, and potentially guiding treatment options.

SKU: TEST-2999 Category:

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