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FGFR1 Gene Jackson-Weiss Syndrome Genetic Test Cost

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

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The FGFR1 Gene Jackson-Weiss Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the FGFR1 gene that are associated with Jackson-Weiss Syndrome. This condition is a rare genetic disorder characterized by craniosynostosis, which involves the premature fusion of skull bones, leading to an abnormal head shape, and can also affect the shape of the feet and hands, among other symptoms. Early detection through genetic testing is crucial for managing the condition and planning appropriate treatments.

DNA Labs UAE provides this comprehensive test at a cost of 4400 AED. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any mutations in the FGFR1 gene that are indicative of Jackson-Weiss Syndrome. The results from this test can help guide clinical decisions, including surgical interventions to correct bone abnormalities and therapies to support developmental outcomes. It is an invaluable tool for families with a history of the syndrome or for individuals showing symptoms, offering a pathway to a clearer diagnosis and tailored care plan.

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FGFR1 Gene Jackson-Weiss Syndrome Genetic Test

At DNA Labs UAE, we offer the FGFR1 Gene Jackson-Weiss syndrome genetic test. This test is designed to identify mutations or variations in the FGFR1 gene that may be responsible for Jackson-Weiss syndrome, a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and foot abnormalities.

Test Details

The FGFR1 gene is associated with Jackson-Weiss syndrome. Our NGS (Next-Generation Sequencing) genetic testing utilizes advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Jackson-Weiss syndrome, this test can help identify any changes or mutations in the FGFR1 gene.

Components

  • Test Name: FGFR1 Gene Jackson-Weiss syndrome 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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the FGFR1 Gene Jackson-Weiss syndrome NGS Genetic DNA 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 with the syndrome.

Test Procedure

The NGS genetic testing for Jackson-Weiss syndrome requires a DNA sample, which is usually obtained through a blood sample or saliva sample. The DNA is then sequenced using NGS technology to identify any changes or mutations in the FGFR1 gene.

Significance

The results of the FGFR1 Gene Jackson-Weiss syndrome genetic test can help confirm a diagnosis of the syndrome and provide information about the specific genetic variant causing the condition. This information is essential for medical management and genetic counseling for individuals and families affected by the syndrome.

Please note that the FGFR1 Gene Jackson-Weiss syndrome genetic test is performed in specialized genetic testing laboratories and must be ordered by a healthcare professional.

Test Name FGFR1 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 FGFR1 Gene Jackson-Weiss syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Jackson-Weiss syndrome NGS Genetic DNA Test gene FGFR1
Test Details

The FGFR1 gene is associated with Jackson-Weiss syndrome, which is a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and foot abnormalities.

NGS (Next-Generation Sequencing) genetic testing refers to a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the context of Jackson-Weiss syndrome, NGS genetic testing can be used to identify mutations or variations in the FGFR1 gene that may be responsible for the disorder.

NGS genetic testing involves obtaining a DNA sample from the individual undergoing testing, typically through a blood sample or saliva sample. The DNA is then sequenced using NGS technology to identify any changes or mutations in the FGFR1 gene. The results of the test can help confirm a diagnosis of Jackson-Weiss syndrome and may also provide information about the specific genetic variant causing the condition.

It’s important to note that NGS genetic testing for Jackson-Weiss syndrome is typically performed in specialized genetic testing laboratories and requires a healthcare professional to order the test. The results of the test can be used to guide medical management and genetic counseling for individuals and families affected by the syndrome.

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