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NRAS Gene Noonan Syndrome Type 6 Genetic Test Cost

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

-21%

The NRAS Gene Noonan Syndrome Type 6 Genetic Test is a specialized diagnostic assessment designed to identify mutations in the NRAS gene, which are implicated in Noonan Syndrome Type 6. This condition is part of a group of disorders known for causing a range of developmental issues, including congenital heart defects, distinctive facial features, and various physical and cognitive developmental delays.

Testing for mutations in the NRAS gene is crucial for accurate diagnosis, allowing for tailored management and treatment plans to be developed for affected individuals. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in a laboratory setting to identify any genetic abnormalities associated with the syndrome.

This specific test is available at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The cost of the NRAS Gene Noonan Syndrome Type 6 Genetic Test at DNA Labs UAE is 4400 AED. This investment can provide invaluable information for affected individuals and their families, guiding medical care and support services to improve quality of life and outcomes.

Description

NRAS Gene Noonan Syndrome Type 6 Genetic Test

Components: NRAS Gene Noonan syndrome type 6 Genetic Test

Price: AED 4400.0

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 NRAS Gene Noonan syndrome type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NRAS Gene Noonan syndrome type 6 NGS Genetic DNA Test gene NRAS

Test Details:

The NRAS gene is associated with Noonan syndrome type 6, which is a genetic disorder characterized by distinctive facial features, heart defects, short stature, and developmental delays. To diagnose this syndrome, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes. In the case of Noonan syndrome type 6, the NGS test would focus on sequencing the NRAS gene to identify any mutations or abnormalities.

The NGS test involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual suspected of having Noonan syndrome type 6. The DNA is then sequenced using NGS technology, which generates a large amount of genetic data. This data is then analyzed to identify any mutations or variants in the NRAS gene that may be causing the syndrome.

The results of the NGS test can help confirm a diagnosis of Noonan syndrome type 6 and provide important information for managing the condition. It can also help with genetic counseling and family planning decisions.

It is important to note that the NGS test for Noonan syndrome type 6 is typically performed by a specialized genetic testing laboratory and should be ordered and interpreted by a healthcare professional with expertise in genetics.

Test Name	NRAS Gene Noonan syndrome type 6 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 NRAS Gene Noonan syndrome type 6 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NRAS Gene Noonan syndrome type 6 NGS Genetic DNA Test gene NRAS
Test Details	The NRAS gene is associated with Noonan syndrome type 6, which is a genetic disorder characterized by distinctive facial features, heart defects, short stature, and developmental delays. To diagnose this syndrome, a Next-Generation Sequencing (NGS) genetic test can be performed. NGS is a high-throughput DNA sequencing technology that allows for the simultaneous analysis of multiple genes. In the case of Noonan syndrome type 6, the NGS test would focus on sequencing the NRAS gene to identify any mutations or abnormalities. The NGS test involves obtaining a DNA sample, typically through a blood or saliva sample, from the individual suspected of having Noonan syndrome type 6. The DNA is then sequenced using NGS technology, which generates a large amount of genetic data. This data is then analyzed to identify any mutations or variants in the NRAS gene that may be causing the syndrome. The results of the NGS test can help confirm a diagnosis of Noonan syndrome type 6 and provide important information for managing the condition. It can also help with genetic counseling and family planning decisions. It is important to note that the NGS test for Noonan syndrome type 6 is typically performed by a specialized genetic testing laboratory and should be ordered and interpreted by a healthcare professional with expertise in genetics.