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FGFR3 Gene Crouzon Syndrome with Acanthosis Nigricans Genetic Test Cost

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

-21%

The FGFR3 Gene Crouzon Syndrome with Acanthosis Nigricans Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the FGFR3 gene, which are linked to Crouzon syndrome with acanthosis nigricans. Crouzon syndrome is a genetic disorder characterized by the premature fusion of certain skull bones, leading to an abnormal shape of the head and face. Acanthosis nigricans, associated with this condition, involves skin changes that produce dark, thickened patches around the body. The test, priced at 4400 AED, utilizes advanced genetic sequencing technologies to identify the specific mutations in the FGFR3 gene, providing crucial information for accurate diagnosis, management, and genetic counseling for affected individuals and their families. This test is pivotal for early intervention and treatment planning, aiming to improve the quality of life for those diagnosed with this rare genetic condition.

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FGFR3 Gene Crouzon Syndrome with Acanthosis Nigricans Genetic Test

At DNA Labs UAE, we offer the FGFR3 Gene Crouzon syndrome with acanthosis nigricans Genetic Test at a cost of AED 4400.0. This test is used to diagnose and assess the risk of Crouzon syndrome with acanthosis nigricans, a genetic disorder characterized by the premature fusion of certain skull bones.

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

Before undergoing the FGFR3 Gene Crouzon syndrome with acanthosis nigricans Genetic Test, it is important to provide the clinical history of the patient. A genetic counseling session will also be conducted to draw a pedigree chart of family members affected by the condition.

Test Details

The FGFR3 gene is associated with Crouzon syndrome, a genetic disorder that affects the fusion of skull bones. This can lead to abnormal facial features, head shape, hearing loss, and dental problems. Acanthosis nigricans, characterized by dark, thickened patches of skin, can also be associated with Crouzon syndrome.

NGS (Next-Generation Sequencing) genetic testing is used to analyze multiple genes simultaneously to identify genetic variations or mutations related to a specific condition. In the case of Crouzon syndrome with acanthosis nigricans, NGS genetic testing helps identify mutations or variations in the FGFR3 gene that may be causing the condition.

This type of genetic testing provides valuable information for diagnosing Crouzon syndrome with acanthosis nigricans, determining the inheritance pattern, assessing the risk of passing on the condition to future generations, guiding treatment decisions, and providing important information for genetic counseling.

Test Name FGFR3 Gene Crouzon syndrome with acanthosis nigricans 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 FGFR3 Gene Crouzon syndrome with acanthosis nigricans NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR3 Gene Crouzon syndrome with acanthosis nigricans NGS Genetic DNA Test gene FGFR3
Test Details

The FGFR3 gene is associated with a condition called Crouzon syndrome, which is a genetic disorder characterized by the premature fusion of certain skull bones. This can result in abnormal facial features and head shape, as well as potential hearing loss and dental problems.

Acanthosis nigricans is a skin condition characterized by dark, thickened patches of skin, often occurring in body folds such as the neck, armpits, and groin. It can be associated with certain underlying medical conditions, including Crouzon syndrome.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously to identify genetic variations or mutations that may be associated with a particular condition. In the case of Crouzon syndrome with acanthosis nigricans, NGS genetic testing can help identify any mutations or variations in the FGFR3 gene that may be causing the condition.

This type of genetic testing can provide valuable information for diagnosing Crouzon syndrome with acanthosis nigricans, as well as for determining the inheritance pattern and assessing the risk of passing on the condition to future generations. It can also help guide treatment decisions and provide important information for genetic counseling.

SKU: TEST-2905 Category:

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