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FGFR1 Gene Pfeiffer Syndrome Genetic Test Cost

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

-21%

The FGFR1 Gene Pfeiffer Syndrome Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the FGFR1 gene, which are linked to Pfeiffer Syndrome. Pfeiffer Syndrome is a rare genetic disorder characterized by the premature fusion of certain skull bones, leading to abnormal shape of the head and face. It may also affect the hands and feet, causing broad, short thumbs and toes. The test plays a crucial role in the early diagnosis and management of the syndrome, enabling healthcare professionals to devise a tailored treatment and intervention plan for affected individuals. Priced at 4400 AED, this test is a valuable resource for families seeking answers about this complex condition, offering them a clear path towards understanding and managing the syndrome’s implications.

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FGFR1 Gene Pfeiffer Syndrome Genetic Test

Welcome to DNA Labs UAE, a leading genetic testing laboratory in the UAE. We offer a comprehensive range of genetic tests, including the FGFR1 Gene Pfeiffer Syndrome Genetic Test.

Test Components

The FGFR1 Gene Pfeiffer Syndrome Genetic Test includes the following components:

  • Test Name: FGFR1 Gene Pfeiffer 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

Before undergoing the FGFR1 Gene Pfeiffer Syndrome Genetic 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 FGFR1 Gene Pfeiffer Syndrome. This will help in better understanding the genetic makeup and inheritance patterns.

Test Details

The FGFR1 gene is associated with Pfeiffer syndrome, a genetic disorder characterized by abnormal development of the skull and face. NGS (Next Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of Pfeiffer syndrome, NGS genetic testing can be used to identify mutations or variations in the FGFR1 gene that may be responsible for the disorder. This type of testing can help with diagnosis, genetic counseling, and potentially guide treatment options.

If you suspect Pfeiffer syndrome or have a family history of the disorder, our FGFR1 Gene Pfeiffer Syndrome Genetic Test can provide valuable insights. Contact DNA Labs UAE today to schedule an appointment or learn more about our genetic testing services.

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

The FGFR1 gene is associated with Pfeiffer syndrome, a genetic disorder characterized by abnormal development of the skull and face. NGS (Next Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. In the context of Pfeiffer syndrome, NGS genetic testing can be used to identify mutations or variations in the FGFR1 gene that may be responsible for the disorder. This type of testing can help with diagnosis, genetic counseling, and potentially guide treatment options.

SKU: TEST-4309 Category:

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