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FGFR1 Gene Craniosynostosis FGFR1 Related Genetic Test Cost

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

-21%

The FGFR1 gene plays a crucial role in the development of bones and tissues in the human body, particularly during the early stages of fetal development. Mutations in this gene can lead to various forms of craniosynostosis, a condition characterized by the premature fusion of skull bones, leading to abnormal skull shape, facial asymmetry, and potential brain development issues. Craniosynostosis associated with FGFR1 mutations can vary in severity and presentation, making accurate diagnosis essential for proper management and intervention.

DNA Labs UAE offers a specialized genetic test aimed at identifying mutations in the FGFR1 gene that are linked to craniosynostosis. This test is an invaluable tool for clinicians and genetic counselors in diagnosing affected individuals, understanding the specific type of craniosynostosis, and providing tailored care and treatment options. It can also be used for family planning and assessing the risk of recurrence in future pregnancies.

The cost of the FGFR1-related genetic test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory for specific mutations in the FGFR1 gene. The process is highly accurate and provides crucial information for the management of craniosynostosis, helping to guide surgical decisions, anticipate potential complications, and offer genetic counseling for affected families.

Given the complexity of craniosynostosis and the importance of early intervention, the FGFR1 genetic test is a vital resource for individuals and families dealing with this condition, offering hope for improved outcomes and quality of life.

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FGFR1 Gene Craniosynostosis FGFR1 related Genetic Test

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 Craniosynostosis, FGFR1 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Craniosynostosis, FGFR1 related NGS Genetic DNA Test gene FGFR1.

Test Details

Craniosynostosis is a condition characterized by the premature fusion of one or more sutures in the skull, leading to abnormal skull shape and potentially affecting brain growth and development. The FGFR1 gene is one of several genes that have been associated with craniosynostosis. FGFR1 codes for a protein called fibroblast growth factor receptor 1, which is involved in cell signaling and regulation of cell growth and differentiation.

An NGS (Next-Generation Sequencing) genetic test is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of FGFR1-related craniosynostosis, an NGS genetic test can identify any mutations or variations in the FGFR1 gene that may be contributing to the development of craniosynostosis.

By identifying specific genetic variants in the FGFR1 gene, an NGS genetic test can help in confirming a diagnosis of FGFR1-related craniosynostosis and provide information about the specific genetic cause of the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment decisions.

It is important to note that FGFR1-related craniosynostosis is a rare condition, and not all cases of craniosynostosis are caused by mutations in the FGFR1 gene. Other genes, such as FGFR2 and FGFR3, have also been associated with craniosynostosis, and a comprehensive genetic test may include analysis of multiple genes to provide a more complete picture of the genetic causes of craniosynostosis.

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

Craniosynostosis is a condition characterized by the premature fusion of one or more sutures in the skull, leading to abnormal skull shape and potentially affecting brain growth and development.

The FGFR1 gene is one of several genes that have been associated with craniosynostosis. FGFR1 codes for a protein called fibroblast growth factor receptor 1, which is involved in cell signaling and regulation of cell growth and differentiation.

An NGS (Next-Generation Sequencing) genetic test is a type of genetic test that can analyze multiple genes simultaneously, providing a comprehensive analysis of an individual’s genetic makeup. In the case of FGFR1-related craniosynostosis, an NGS genetic test can identify any mutations or variations in the FGFR1 gene that may be contributing to the development of craniosynostosis.

By identifying specific genetic variants in the FGFR1 gene, an NGS genetic test can help in confirming a diagnosis of FGFR1-related craniosynostosis and provide information about the specific genetic cause of the condition. This information can be useful for genetic counseling, family planning, and potentially guiding treatment decisions.

It is important to note that FGFR1-related craniosynostosis is a rare condition, and not all cases of craniosynostosis are caused by mutations in the FGFR1 gene. Other genes, such as FGFR2 and FGFR3, have also been associated with craniosynostosis, and a comprehensive genetic test may include analysis of multiple genes to provide a more complete picture of the genetic causes of craniosynostosis.

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