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FGFR2 Gene Pfeiffer Syndrome Genetic Test

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

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The FGFR2 Gene Pfeiffer Syndrome Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FGFR2 gene, which are associated with Pfeiffer Syndrome. Pfeiffer Syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones, leading to abnormalities in the shape of the head and face, along with issues related to the hands and feet. This condition is inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the FGFR2 gene can cause the disorder.

Conducted at DNA Labs UAE, this genetic test is an essential tool for accurate diagnosis, allowing for early intervention and management of the syndrome. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any mutations in the FGFR2 gene that are indicative of Pfeiffer Syndrome.

The cost of the FGFR2 Gene Pfeiffer Syndrome Genetic Test at DNA Labs UAE is 4400 AED. The price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the FGFR2 gene. This test is crucial for affected families, providing them with the necessary information for genetic counseling, understanding the risk of recurrence in future pregnancies, and exploring potential treatment options or interventions for managing the symptoms associated with Pfeiffer Syndrome.

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FGFR2 Gene Pfeiffer Syndrome Genetic Test

Are you concerned about Pfeiffer syndrome and its genetic implications? DNA Labs UAE offers the FGFR2 Gene Pfeiffer Syndrome Genetic Test at an affordable price of 4400.0 AED.

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

Before undergoing the FGFR2 Gene Pfeiffer Syndrome Genetic Test, it is essential 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 by Pfeiffer syndrome. This will help in identifying potential genetic markers associated with the FGFR2 gene.

Test Details

The FGFR2 gene is closely linked to Pfeiffer syndrome, a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and other skeletal abnormalities. To analyze the presence of mutations or variations in the FGFR2 gene, we utilize Next-Generation Sequencing (NGS) technology.

NGS is a cutting-edge genetic testing method that allows for the simultaneous analysis of multiple genes. By evaluating an individual’s genetic makeup comprehensively, this test aids in confirming a diagnosis, predicting disease severity, and guiding treatment decisions.

Don’t let the uncertainty surrounding Pfeiffer syndrome linger. Take advantage of our FGFR2 Gene Pfeiffer Syndrome Genetic Test to gain valuable insights into your genetic profile. Contact DNA Labs UAE today to schedule an appointment.

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

The FGFR2 gene is associated with Pfeiffer syndrome, which is a rare genetic disorder characterized by craniosynostosis (premature fusion of the skull bones) and other skeletal abnormalities.

NGS (Next-Generation Sequencing) is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive evaluation of an individual’s genetic makeup. In the context of Pfeiffer syndrome, an NGS genetic test can detect mutations or variations in the FGFR2 gene that may be responsible for the condition. This test can help in confirming a diagnosis, predicting disease severity, and guiding treatment decisions.

SKU: TEST-4310 Category:

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