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NAGLU Gene Mucopolysaccharidosis Type 3B Genetic Test Cost

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

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The NAGLU Gene Mucopolysaccharidosis Type 3B Genetic Test is a specialized diagnostic procedure designed to identify mutations in the NAGLU gene, which are responsible for causing Mucopolysaccharidosis Type 3B (MPS IIIB), also known as Sanfilippo Syndrome Type B. This condition is a rare genetic disorder that affects the body’s ability to break down large sugar molecules called glycosaminoglycans, leading to their accumulation in cells and tissues, which can cause severe neurological symptoms and physical impairments.

The test is conducted through DNA analysis, where a sample of the patient’s blood or saliva is collected and examined for specific genetic alterations in the NAGLU gene. Identifying these mutations can confirm a diagnosis of MPS IIIB, which is crucial for early intervention, management strategies, and genetic counseling for affected families.

Performed at DNA Labs UAE, a leading facility in genetic testing, the cost of the NAGLU Gene Mucopolysaccharidosis Type 3B Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to detect the genetic variations associated with this condition, providing essential information for healthcare providers, patients, and their families to navigate the challenges of MPS IIIB.

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NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test

At DNA Labs UAE, we offer the NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test to help diagnose and identify mutations in the NAGLU gene. This test is crucial for individuals suspected of having Mucopolysaccharidosis type 3B (MPS 3B), also known as Sanfilippo syndrome type B.

Test Details

The NAGLU gene is responsible for producing an enzyme called alpha-N-acetylglucosaminidase. Mutations in this gene can cause MPS 3B, an autosomal recessive disorder characterized by the accumulation of glycosaminoglycans (GAGs) in the body’s cells, particularly in the brain and other organs.

Our NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze the DNA sequence of a person’s genes. This advanced genetic testing method can identify mutations in the NAGLU gene, confirm a diagnosis of MPS 3B, and determine the specific genetic changes responsible for the disease.

NGS genetic testing is a powerful tool for diagnosing genetic disorders as it can analyze multiple genes simultaneously and detect various types of genetic changes. This comprehensive approach allows for a more accurate and efficient diagnosis of MPS 3B.

Test Components and Price

  • Test Name: NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test
  • Components: NGS Technology
  • Price: 4400.0 AED
  • Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
  • Report Delivery: 3 to 4 Weeks
  • Test Type: Metabolic Disorders
  • Doctor: General Physician
  • Test Department: Genetics
  • Pre Test Information: Clinical History of Patient who is going for NAGLU Gene Mucopolysaccharidosis type 3B NGS Genetic DNA Test, Genetic Counselling session to draw a pedigree chart of family members affected with MPS 3B

Why Choose NGS Genetic Testing?

NGS genetic testing for the NAGLU gene in individuals suspected of having MPS 3B provides valuable information for diagnosis, genetic counseling, and potential treatment options. With its ability to analyze multiple genes simultaneously and detect various types of genetic changes, NGS genetic testing offers a comprehensive approach to accurately diagnose MPS 3B.

By identifying the specific genetic changes responsible for the disease, NGS genetic testing enables healthcare professionals to provide personalized treatment plans and genetic counseling for patients and their families.

Conclusion

The NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test offered by DNA Labs UAE is a powerful tool for diagnosing MPS 3B. With its NGS technology, this test can accurately identify mutations in the NAGLU gene, confirm a diagnosis, and provide valuable information for genetic counseling and potential treatment options.

If you suspect that you or a loved one may have MPS 3B, we encourage you to consult with a general physician and consider undergoing the NAGLU Gene Mucopolysaccharidosis type 3B Genetic Test. Early diagnosis and intervention can make a significant difference in managing the condition and improving quality of life.

Test Name NAGLU Gene Mucopolysaccharidosis type 3B 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 NAGLU Gene Mucopolysaccharidosis type 3B NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Mucopolysaccharidosis type 3B
Test Details

The NAGLU gene is responsible for producing an enzyme called alpha-N-acetylglucosaminidase. Mutations in this gene can cause a rare genetic disorder called Mucopolysaccharidosis type 3B (MPS 3B), also known as Sanfilippo syndrome type B.

MPS 3B is an autosomal recessive disorder, meaning that both copies of the NAGLU gene must have mutations for the disease to occur. This condition leads to the accumulation of certain complex sugar molecules called glycosaminoglycans (GAGs) in the body’s cells, particularly in the brain and other organs.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technologies to analyze the DNA sequence of a person’s genes. In the context of MPS 3B, NGS genetic testing can be used to identify mutations in the NAGLU gene. This test can help confirm a diagnosis of MPS 3B and determine the specific genetic changes responsible for the disease.

NGS genetic testing is a powerful tool for diagnosing genetic disorders because it can analyze multiple genes simultaneously and detect various types of genetic changes, including small point mutations, insertions, deletions, and rearrangements. This comprehensive approach allows for a more accurate and efficient diagnosis of MPS 3B.

Overall, NGS genetic testing for the NAGLU gene in individuals suspected of having MPS 3B can provide valuable information for diagnosis, genetic counseling, and potential treatment options.

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