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FGFR2 Gene Jackson-Weiss Syndrome Genetic Test Cost

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

-21%

The FGFR2 Gene Jackson-Weiss Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the FGFR2 gene, which are known to cause Jackson-Weiss Syndrome. This condition is a rare genetic disorder characterized by abnormalities in the development of the skull, facial features, and, occasionally, the feet. Early detection through this genetic test can play a crucial role in managing and treating the syndrome effectively.

DNA Labs UAE, a leading facility in genetic testing, offers this comprehensive test at a cost of 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the lab for the presence of specific mutations in the FGFR2 gene. Results from this test can provide valuable information for affected individuals and their families regarding the diagnosis, prognosis, and potential treatment options for Jackson-Weiss Syndrome, thereby facilitating informed medical and personal decisions.

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FGFR2 Gene Jackson-Weiss syndrome Genetic Test

Cost: AED 4400.0

Symptoms and Diagnosis

The FGFR2 gene is associated with Jackson-Weiss syndrome, a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and foot abnormalities.

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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

A Genetic Counselling session is required to draw a pedigree chart of family members affected with FGFR2 Gene Jackson-Weiss syndrome NGS Genetic DNA Test gene FGFR2. It is important to provide the clinical history of the patient who is going for the test.

Test Details

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes to identify any mutations or variations that may be associated with a particular condition. In the case of Jackson-Weiss syndrome, an NGS genetic test would involve sequencing the FGFR2 gene to detect any genetic changes that could be causing the disorder.

This type of genetic testing can help confirm a diagnosis of Jackson-Weiss syndrome and provide information about the specific mutation in the FGFR2 gene. It can also be used for genetic counseling and to assess the risk of passing the condition on to future generations.

Test Name FGFR2 Gene Jackson-Weiss syndrome 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 FGFR2 Gene Jackson-Weiss syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Jackson-Weiss syndrome NGS Genetic DNA Test gene FGFR2
Test Details

The FGFR2 gene is associated with Jackson-Weiss syndrome, a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and foot abnormalities.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of genes to identify any mutations or variations that may be associated with a particular condition. In the case of Jackson-Weiss syndrome, an NGS genetic test would involve sequencing the FGFR2 gene to detect any genetic changes that could be causing the disorder.

This type of genetic testing can help confirm a diagnosis of Jackson-Weiss syndrome and provide information about the specific mutation in the FGFR2 gene. It can also be used for genetic counseling and to assess the risk of passing the condition on to future generations.

SKU: TEST-4180 Category:

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