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NBN Gene Nijmegen Breakage Syndrome Genetic Test Cost

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

-21%

The NBN Gene Nijmegen Breakage Syndrome Genetic Test is a specialized diagnostic procedure designed to detect mutations in the NBN gene, which are indicative of Nijmegen Breakage Syndrome (NBS). NBS is a rare autosomal recessive genetic disorder characterized by microcephaly, a distinct facial appearance, growth retardation, immunodeficiency, and an increased risk of cancer, particularly lymphoma. The test is crucial for the early identification of the syndrome, allowing for appropriate medical management and surveillance for complications associated with the condition.

Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the NBN gene to identify the specific mutations associated with Nijmegen Breakage Syndrome. The cost of the test is set at 4400 AED, reflecting the intricate technology and expertise required to accurately detect and interpret the genetic variations responsible for the syndrome.

By opting for the NBN Gene Nijmegen Breakage Syndrome Genetic Test at DNA Labs UAE, patients and their families can gain valuable insights into their genetic health, enabling informed decisions regarding their medical care and the management of the syndrome’s various health implications.

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NBN Gene Nijmegen Breakage Syndrome Genetic Test

At DNA Labs UAE, we offer the NBN Gene Nijmegen breakage syndrome Genetic Test at a cost of AED 4400.0.

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: Dysmorphology
  • Doctor: Pediatrics
  • Test Department: Genetics

Pre Test Information

Before undergoing the NBN Gene Nijmegen breakage syndrome NGS Genetic DNA 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 NBN Gene Nijmegen breakage syndrome NGS Genetic DNA Test gene NBN.

Test Details

The NBN Gene Nijmegen breakage syndrome NGS genetic test is a type of genetic test that detects mutations in the NBN gene, which is associated with Nijmegen breakage syndrome (NBS). NBS is a rare genetic disorder characterized by physical and developmental abnormalities such as growth retardation, microcephaly, immunodeficiency, and an increased risk of certain cancers.

The NGS technology used in this test allows for rapid and comprehensive analysis of the NBN gene, enabling the identification of various types of mutations including insertions, deletions, and single nucleotide variants.

This test can confirm a diagnosis of NBS in individuals with clinical symptoms and can also be used for carrier testing in individuals with a family history of NBS. The results of this genetic test can provide valuable information for genetic counseling, management, and treatment decisions for individuals with NBS and their families.

It is important to note that this test is typically performed in specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics.

Test Name NBN Gene Nijmegen breakage syndrome 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 Dysmorphology
Doctor Pediatrics
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for NBN Gene Nijmegen breakage syndrome NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with NBN Gene Nijmegen breakage syndrome NGS Genetic DNA Test gene NBN
Test Details

NBN Gene Nijmegen breakage syndrome NGS genetic test is a type of genetic test that is used to detect mutations in the NBN gene, which is associated with Nijmegen breakage syndrome (NBS). NBS is a rare genetic disorder characterized by a variety of physical and developmental abnormalities, including growth retardation, microcephaly (small head size), immunodeficiency, and an increased risk of developing certain types of cancer.

The NGS (next-generation sequencing) technology used in this test allows for the rapid and comprehensive analysis of the NBN gene, enabling the identification of various types of mutations, including small insertions, deletions, and single nucleotide variants. This test can help confirm a diagnosis of NBS in individuals with clinical symptoms and can also be used for carrier testing in individuals with a family history of NBS.

The results of the NBN Gene Nijmegen breakage syndrome NGS genetic test can provide valuable information for genetic counseling, management, and treatment decisions for individuals with NBS and their families. It is important to note that this test is typically performed in specialized genetic testing laboratories and should be ordered and interpreted by healthcare professionals with expertise in genetics.

SKU: TEST-4275 Category:

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