Sale!

GLUL Gene Glutamine deficiency congenital Genetic Test Cost

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

-21%

The “GLUL Gene Glutamine Deficiency Congenital Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the GLUL gene, which can lead to congenital glutamine deficiency. This condition is rare and affects the body’s ability to synthesize glutamine, an amino acid essential for various bodily functions, including immune system support, gut health, and brain function. Early detection through this genetic test can be crucial for managing symptoms and improving the quality of life for affected individuals. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for any genetic abnormalities associated with this condition. The cost of the test is 4400 AED, reflecting the specialized analysis and detailed genetic counseling that accompanies the testing process. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetics, ensuring accurate and reliable results for those undergoing testing.

Description

GLUL Gene Glutamine deficiency congenital Genetic Test

Test Name: GLUL Gene Glutamine deficiency congenital Genetic Test

Components: Glutamine synthetase enzyme deficiency analysis

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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GLUL Gene Glutamine deficiency, congenital NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Glutamine deficiency, congenital.

Test Details: GLUL gene refers to the gene that encodes the enzyme glutamine synthetase. Glutamine deficiency, congenital (CDG) is a rare genetic disorder characterized by a deficiency in the enzyme glutamine synthetase, resulting in impaired conversion of glutamate to glutamine. NGS (Next-Generation Sequencing) genetic test is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes. In the context of GLUL gene and glutamine deficiency, congenital, NGS genetic test can be used to identify mutations or variants in the GLUL gene that may be responsible for the disorder. NGS genetic testing involves sequencing the DNA of an individual to detect any changes or mutations in the GLUL gene. This test can help in confirming a diagnosis of glutamine deficiency, congenital and provide information about the specific genetic variant causing the disorder. Genetic testing can be useful for individuals with symptoms suggestive of glutamine deficiency, congenital, as well as for family members of affected individuals who may be at risk of carrying the same genetic variant. The results of the NGS genetic test can help in understanding the underlying cause of the disorder, facilitating appropriate management and genetic counseling.

Test Name	GLUL Gene Glutamine deficiency congenital 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	Metabolic Disorders
Doctor	General Physician
Test Department:	Genetics
Pre Test Information	Clinical History of Patient who is going for GLUL Gene Glutamine deficiency, congenital NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glutamine deficiency, congenital
Test Details	GLUL gene refers to the gene that encodes the enzyme glutamine synthetase. Glutamine deficiency, congenital (CDG) is a rare genetic disorder characterized by a deficiency in the enzyme glutamine synthetase, resulting in impaired conversion of glutamate to glutamine. NGS (Next-Generation Sequencing) genetic test is a high-throughput sequencing technology that allows for the simultaneous analysis of multiple genes. In the context of GLUL gene and glutamine deficiency, congenital, NGS genetic test can be used to identify mutations or variants in the GLUL gene that may be responsible for the disorder. NGS genetic testing involves sequencing the DNA of an individual to detect any changes or mutations in the GLUL gene. This test can help in confirming a diagnosis of glutamine deficiency, congenital and provide information about the specific genetic variant causing the disorder. Genetic testing can be useful for individuals with symptoms suggestive of glutamine deficiency, congenital, as well as for family members of affected individuals who may be at risk of carrying the same genetic variant. The results of the NGS genetic test can help in understanding the underlying cause of the disorder, facilitating appropriate management and genetic counseling.