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GYS2 Gene Glycogen storage disease type 0 Genetic Test Cost

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

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The GYS2 gene is crucial in the regulation and synthesis of glycogen in the liver, playing a pivotal role in maintaining blood sugar levels during fasting periods. Mutations in the GYS2 gene can lead to Glycogen Storage Disease type 0 (GSD0), a rare metabolic disorder characterized by fasting hypoglycemia, high blood ketones, and low blood sugar levels upon waking.

DNA Labs UAE offers a comprehensive genetic test for the GYS2 gene to diagnose Glycogen Storage Disease type 0. This test is particularly valuable for individuals presenting symptoms of GSD0 or those with a family history of the disorder, as early diagnosis can significantly impact management and treatment strategies.

The test cost is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the GYS2 gene. Conducted in a state-of-the-art laboratory by a team of specialized geneticists and technicians, this test involves analyzing the patient’s DNA to detect any genetic variations responsible for the disease.

By opting for this genetic test at DNA Labs UAE, patients and their families can gain crucial insights into their genetic health, enabling informed decisions regarding lifestyle adjustments, treatment options, and family planning.

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GYS2 Gene Glycogen Storage Disease Type 0 Genetic Test

At DNA Labs UAE, we offer the GYS2 Gene Glycogen Storage Disease Type 0 Genetic Test. This test is designed to diagnose and provide information about Glycogen Storage Disease Type 0 (GSD0), a rare metabolic disorder associated with the GYS2 gene.

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

Before undergoing the GYS2 Gene Glycogen Storage Disease Type 0 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by Glycogen Storage Disease Type 0.

Test Details

Glycogen Storage Disease Type 0 (GSD0) is a rare metabolic disorder characterized by the inability to break down glycogen into glucose, resulting in low blood sugar levels. The GYS2 gene is associated with this genetic disorder.

The GYS2 Gene Glycogen Storage Disease Type 0 Genetic Test utilizes Next-Generation Sequencing (NGS) technology to analyze multiple genes simultaneously. Specifically, it identifies mutations or variations in the GYS2 gene that may be responsible for the disorder. The test involves collecting a DNA sample, typically through a blood sample or cheek swab, and analyzing the DNA sequence of the GYS2 gene using advanced sequencing technologies.

The results of the test can aid in the diagnosis of GSD0 and provide information about the specific genetic variant causing the disease. Additionally, NGS genetic testing can assist in predicting disease progression and guiding treatment decisions. It can also be used for carrier testing to determine if an individual carries a mutation in the GYS2 gene, which may be passed on to future generations.

It is crucial to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. These professionals can offer a comprehensive understanding of the test results, explain the implications for the individual and their family, and provide guidance for managing the condition.

Test Name GYS2 Gene Glycogen storage disease type 0 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 GYS2 Gene Glycogen storage disease type 0 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Glycogen storage disease type 0
Test Details

The GYS2 gene is associated with a genetic disorder called Glycogen Storage Disease Type 0 (GSD0). GSD0 is a rare metabolic disorder characterized by an inability to break down glycogen into glucose, leading to low blood sugar levels.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. In the context of GSD0, NGS genetic testing can identify mutations or variations in the GYS2 gene that may be responsible for the disorder.

This type of genetic test involves collecting a DNA sample, usually through a blood sample or cheek swab, and analyzing the DNA sequence of the GYS2 gene using advanced sequencing technologies. The results of the test can help diagnose GSD0 and provide information about the specific genetic variant causing the disease.

NGS genetic testing for GSD0 can be helpful in confirming a clinical diagnosis, predicting disease progression, and guiding treatment decisions. It can also be used for carrier testing to determine if an individual carries a mutation in the GYS2 gene, which could be passed on to future generations.

It is important to note that genetic testing should be performed and interpreted by healthcare professionals with expertise in genetics and genetic counseling. They can provide a comprehensive understanding of the test results, explain the implications for the individual and their family, and offer guidance for managing the condition.

SKU: TEST-2354 Category:

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