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FGFR2 Gene Saethre-Chotzen Syndrome Genetic Test Cost

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

-21%

The FGFR2 Gene Saethre-Chotzen Syndrome Genetic Test is a specialized diagnostic procedure designed to detect mutations in the FGFR2 gene, which are associated with Saethre-Chotzen Syndrome (SCS). Saethre-Chotzen Syndrome is a congenital condition characterized by craniosynostosis (premature fusion of skull bones), leading to abnormal skull shape, facial asymmetry, and potentially impacting brain development. Other features may include minor limb abnormalities and partial webbing of the fingers or toes. The condition varies in severity and other manifestations can include short stature, hearing loss, and dental problems.

This genetic test involves analyzing the patient’s DNA to identify mutations in the FGFR2 gene that are known to cause Saethre-Chotzen Syndrome. Early and accurate diagnosis through this test can enable appropriate medical intervention, guidance for family planning, and genetic counseling for affected families.

The test is available at DNA Labs UAE, a leading facility specializing in genetic and molecular diagnostics. The cost of the FGFR2 Gene Saethre-Chotzen Syndrome Genetic Test is 4400 AED. Conducted in a state-of-the-art laboratory by skilled geneticists and technicians, this test offers families vital information for the management of the syndrome, potentially improving the quality of life for those affected.

Description

FGFR2 Gene Saethre-Chotzen syndrome Genetic Test

Test Name: FGFR2 Gene Saethre-Chotzen syndrome 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 FGFR2 Gene Saethre-Chotzen syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Saethre-Chotzen syndrome NGS Genetic DNA Test gene FGFR2

Test Details: The FGFR2 gene is associated with a genetic disorder called Saethre-Chotzen syndrome. Saethre-Chotzen syndrome is a rare genetic condition characterized by craniosynostosis (premature fusion of the skull bones), distinctive facial features, and hand and foot abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Saethre-Chotzen syndrome, NGS genetic testing can be used to identify mutations or variations in the FGFR2 gene that are associated with the condition. By analyzing the FGFR2 gene using NGS, healthcare professionals can determine if an individual has mutations or variations in this gene that are causative or associated with Saethre-Chotzen syndrome. This information can be used for diagnostic purposes, genetic counseling, and potentially to guide treatment decisions.

Test Name	FGFR2 Gene Saethre-Chotzen 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 Saethre-Chotzen syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGFR2 Gene Saethre-Chotzen syndrome NGS Genetic DNA Test gene FGFR2
Test Details	The FGFR2 gene is associated with a genetic disorder called Saethre-Chotzen syndrome. Saethre-Chotzen syndrome is a rare genetic condition characterized by craniosynostosis (premature fusion of the skull bones), distinctive facial features, and hand and foot abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of Saethre-Chotzen syndrome, NGS genetic testing can be used to identify mutations or variations in the FGFR2 gene that are associated with the condition. By analyzing the FGFR2 gene using NGS, healthcare professionals can determine if an individual has mutations or variations in this gene that are causative or associated with Saethre-Chotzen syndrome. This information can be used for diagnostic purposes, genetic counseling, and potentially to guide treatment decisions.