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SCARF2 Gene Van den Ende-Gupta Syndrome Genetic Test Cost

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

-21%

The SCARF2 gene Van den Ende-Gupta syndrome genetic test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the SCARF2 gene, which are associated with Van den Ende-Gupta syndrome (VEGS). This rare genetic disorder is characterized by craniofacial, skeletal, and limb abnormalities, with patients often presenting with features such as malar hypoplasia, arachnodactyly, and camptodactyly, among others. The test aims to provide a definitive diagnosis for individuals displaying symptoms suggestive of VEGS, facilitating appropriate management and genetic counseling.

Performed at DNA Labs UAE, a facility renowned for its advanced genetic testing capabilities, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the SCARF2 gene. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed reporting provided by the lab.

This genetic test is crucial for affected families, as it not only confirms the diagnosis but also aids in understanding the inheritance patterns and potential risks for future offspring. Early diagnosis through the SCARF2 gene test can lead to better management of the syndrome’s symptoms and improvements in the quality of life for those affected.

Description

SCARF2 Gene Van den Ende-Gupta syndrome Genetic Test

Test Name: SCARF2 Gene Van den Ende-Gupta syndrome Genetic Test

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

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 SCARF2 Gene Van den Ende-Gupta syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCARF2 Gene Van den Ende-Gupta syndrome NGS Genetic DNA Test gene SCARF2

Test Details: The SCARF2 gene is associated with a rare genetic disorder called Van den Ende-Gupta syndrome (VDEGS). This syndrome is characterized by a combination of craniofacial abnormalities, joint contractures, and other developmental anomalies. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of a person’s genetic makeup. In the case of VDEGS, NGS genetic testing can be used to identify mutations or variations in the SCARF2 gene that may be responsible for the syndrome. The NGS test involves obtaining a DNA sample from the individual, typically through a blood or saliva sample. The DNA is then sequenced using advanced technology, which allows for the detection of genetic variations in the SCARF2 gene. The results of the test can help confirm a diagnosis of VDEGS and provide valuable information for genetic counseling and management of the condition. It is important to note that NGS genetic testing is typically conducted in specialized laboratories and requires a healthcare professional’s referral. The test results should be interpreted by a geneticist or genetic counselor who can provide appropriate guidance and support based on the individual’s specific genetic profile.

Test Name	SCARF2 Gene Van den Ende-Gupta 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 SCARF2 Gene Van den Ende-Gupta syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCARF2 Gene Van den Ende-Gupta syndrome NGS Genetic DNA Test gene SCARF2
Test Details	The SCARF2 gene is associated with a rare genetic disorder called Van den Ende-Gupta syndrome (VDEGS). This syndrome is characterized by a combination of craniofacial abnormalities, joint contractures, and other developmental anomalies. NGS (Next-Generation Sequencing) genetic testing is a method used to analyze multiple genes simultaneously, allowing for a more comprehensive evaluation of a person’s genetic makeup. In the case of VDEGS, NGS genetic testing can be used to identify mutations or variations in the SCARF2 gene that may be responsible for the syndrome. The NGS test involves obtaining a DNA sample from the individual, typically through a blood or saliva sample. The DNA is then sequenced using advanced technology, which allows for the detection of genetic variations in the SCARF2 gene. The results of the test can help confirm a diagnosis of VDEGS and provide valuable information for genetic counseling and management of the condition. It is important to note that NGS genetic testing is typically conducted in specialized laboratories and requires a healthcare professional’s referral. The test results should be interpreted by a geneticist or genetic counselor who can provide appropriate guidance and support based on the individual’s specific genetic profile.