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FGFR1 Gene Trigonocephaly Type 1 Genetic Test Cost

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

-21%

The FGFR1 Gene Trigonocephaly Type 1 Genetic Test is a specialized diagnostic procedure designed to detect mutations in the FGFR1 gene, which are associated with Trigonocephaly Type 1, a rare genetic disorder characterized by a triangularly shaped forehead caused by the premature fusion of the metopic suture. This condition may lead to developmental delays, cognitive impairment, and physical deformities. The test is crucial for early diagnosis and intervention, allowing for tailored treatment and management plans for affected individuals.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific mutations in the FGFR1 gene. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results accurately.

Early diagnosis through the FGFR1 Gene Trigonocephaly Type 1 Genetic Test can significantly impact the quality of life for individuals with this condition, guiding healthcare professionals in providing the most effective treatments and support for managing symptoms and preventing complications.

Description

FGFR1 Gene Trigonocephaly type 1 Genetic Test

Test Name: FGFR1 Gene Trigonocephaly type 1 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

Price: 4400.0 AED

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 Trigonocephaly type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Trigonocephaly type 1 NGS Genetic DNA Test gene FGFR1

Test Details:

The FGFR1 gene is a gene that provides instructions for making a protein called fibroblast growth factor receptor 1. This protein is involved in the development and maintenance of various tissues and organs in the body. Trigonocephaly type 1 is a craniofacial condition characterized by a triangular-shaped head due to the premature fusion of certain skull bones. This condition can be caused by mutations in the FGFR1 gene.

NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, including the FGFR1 gene, to identify any mutations or variations that may be present. Therefore, an FGFR1 gene trigonocephaly type 1 NGS genetic test would involve sequencing the FGFR1 gene to identify any mutations or variations that may be associated with trigonocephaly type 1. This test can help in the diagnosis and management of individuals with this condition.

Test Name	FGFR1 Gene Trigonocephaly type 1 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 Trigonocephaly type 1 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR1 Gene Trigonocephaly type 1 NGS Genetic DNA Test gene FGFR1
Test Details	The FGFR1 gene is a gene that provides instructions for making a protein called fibroblast growth factor receptor 1. This protein is involved in the development and maintenance of various tissues and organs in the body. Trigonocephaly type 1 is a craniofacial condition characterized by a triangular-shaped head due to the premature fusion of certain skull bones. This condition can be caused by mutations in the FGFR1 gene. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze the DNA sequence of an individual’s genes. It allows for the simultaneous analysis of multiple genes, including the FGFR1 gene, to identify any mutations or variations that may be present. Therefore, an FGFR1 gene trigonocephaly type 1 NGS genetic test would involve sequencing the FGFR1 gene to identify any mutations or variations that may be associated with trigonocephaly type 1. This test can help in the diagnosis and management of individuals with this condition.