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GLYCTK Gene D-glyceric aciduria Genetic Test Cost

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

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The GLYCTK Gene D-glyceric aciduria Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the GLYCTK gene, which are associated with D-glyceric aciduria, a rare metabolic disorder. This condition is characterized by elevated levels of D-glyceric acid in the urine, blood, and cerebrospinal fluid, potentially leading to various neurological symptoms, developmental delays, and metabolic complications. The test involves analyzing the patient’s DNA to identify any genetic abnormalities in the GLYCTK gene that may indicate the presence of D-glyceric aciduria.

Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a crucial resource for individuals suspected of having this condition or for families with a history of metabolic disorders seeking a definitive diagnosis. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed report provided, which includes specific mutations identified and interpretation of the results in the context of the patient’s health and family history. This information is vital for developing an effective management plan, offering genetic counseling, and understanding the risk of passing the condition to future generations.

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GLYCTK Gene D-glyceric aciduria Genetic Test

Test Name: GLYCTK Gene D-glyceric aciduria 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: Metabolic Disorders

Doctor: General Physician

Test Department: Genetics

Pre Test Information: Clinical History of Patient who is going for GLYCTK Gene D-glyceric aciduria NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with D-glyceric aciduria.

Test Details

The GLYCTK gene is responsible for providing instructions to produce the enzyme called glycerate kinase. This enzyme is involved in a metabolic pathway that converts D-glycerate, a molecule derived from the breakdown of certain amino acids, into glycerate-2-phosphate.

D-glyceric aciduria is a rare genetic disorder characterized by the inability to properly metabolize D-glycerate, leading to the accumulation of this molecule in the body. This condition is caused by mutations in the GLYCTK gene, which result in reduced or absent activity of the glycerate kinase enzyme.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of D-glyceric aciduria, NGS can be used to sequence the GLYCTK gene and identify any mutations or variants that may be present.

By identifying mutations in the GLYCTK gene, NGS genetic testing can help diagnose D-glyceric aciduria and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder.

Test Name GLYCTK Gene D-glyceric aciduria 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 GLYCTK Gene D-glyceric aciduria NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with D-glyceric aciduria
Test Details

The GLYCTK gene is responsible for providing instructions to produce the enzyme called glycerate kinase. This enzyme is involved in a metabolic pathway that converts D-glycerate, a molecule derived from the breakdown of certain amino acids, into glycerate-2-phosphate.

D-glyceric aciduria is a rare genetic disorder characterized by the inability to properly metabolize D-glycerate, leading to the accumulation of this molecule in the body. This condition is caused by mutations in the GLYCTK gene, which result in reduced or absent activity of the glycerate kinase enzyme.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. In the case of D-glyceric aciduria, NGS can be used to sequence the GLYCTK gene and identify any mutations or variants that may be present.

By identifying mutations in the GLYCTK gene, NGS genetic testing can help diagnose D-glyceric aciduria and provide valuable information for genetic counseling and management of the condition. It can also be used for carrier testing in individuals with a family history of the disorder.

SKU: TEST-2277 Category:

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