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NEU1 Gene Neuraminidase Deficiency Genetic Test Cost

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

-21%

The NEU1 Gene Neuraminidase Deficiency Genetic Test is a specialized diagnostic tool designed to detect mutations in the NEU1 gene, which are associated with Sialidosis, a rare lysosomal storage disease. Sialidosis is characterized by a deficiency of the enzyme neuraminidase, leading to a buildup of sialic acid-rich oligosaccharides in the body. This condition manifests in various forms, ranging from mild to severe symptoms, including vision impairment, muscle weakness, and neurological complications.

Performed at DNA Labs UAE, this genetic test involves analyzing the patient’s DNA to identify mutations in the NEU1 gene that can cause the disease. The test is crucial for early diagnosis, allowing for appropriate management and treatment strategies to be implemented, potentially improving the quality of life for affected individuals.

The cost of the NEU1 Gene Neuraminidase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test and the sophisticated technology and expertise required to accurately identify mutations in the NEU1 gene. Patients interested in this test should consult with a healthcare professional to understand its benefits and implications fully.

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NEU1 Gene Neuraminidase Deficiency Genetic Test

Are you concerned about Neuraminidase deficiency? DNA Labs UAE offers the NEU1 Gene Neuraminidase deficiency genetic test at an affordable cost of AED 4400.0. This test can help diagnose and understand the genetic basis of this rare genetic disorder.

Test Details

NEU1 gene neuraminidase deficiency is a rare genetic disorder characterized by a deficiency or dysfunction of the NEU1 gene, which codes for the enzyme neuraminidase. Neuraminidase is responsible for breaking down certain molecules called sialic acids in the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. It allows for the rapid and cost-effective analysis of a large number of genes, including the NEU1 gene.

NGS genetic testing for NEU1 gene neuraminidase deficiency involves sequencing the NEU1 gene to identify any mutations or variations that may be causing the deficiency or dysfunction of the neuraminidase enzyme. This can help in diagnosing the condition and understanding its genetic basis.

NGS genetic testing can also be used for carrier testing, prenatal testing, or to identify potential therapeutic targets for individuals with NEU1 gene neuraminidase deficiency.

It is important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or geneticist, who can provide appropriate counseling and interpretation of the results.

Test Components

  • 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: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics

Pre Test Information

Prior to undergoing the NEU1 Gene Neuraminidase deficiency NGS Genetic DNA Test, it is recommended to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with Neuraminidase deficiency.

Take control of your health and get the NEU1 Gene Neuraminidase deficiency genetic test at DNA Labs UAE today!

Test Name NEU1 Gene Neuraminidase deficiency 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 NEU1 Gene Neuraminidase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Neuraminidase deficiency
Test Details

NEU1 gene neuraminidase deficiency is a rare genetic disorder characterized by a deficiency or dysfunction of the NEU1 gene, which codes for the enzyme neuraminidase. Neuraminidase is responsible for breaking down certain molecules called sialic acids in the body.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses high-throughput sequencing technologies to analyze multiple genes simultaneously. It allows for the rapid and cost-effective analysis of a large number of genes, including the NEU1 gene.

NGS genetic testing for NEU1 gene neuraminidase deficiency involves sequencing the NEU1 gene to identify any mutations or variations that may be causing the deficiency or dysfunction of the neuraminidase enzyme. This can help in diagnosing the condition and understanding its genetic basis.

NGS genetic testing can also be used for carrier testing, prenatal testing, or to identify potential therapeutic targets for individuals with NEU1 gene neuraminidase deficiency.

It is important to note that genetic testing should be done under the guidance of a healthcare professional, such as a genetic counselor or geneticist, who can provide appropriate counseling and interpretation of the results.