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PALB2 Gene Fanconi anemia type N Genetic Test Cost

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

-21%

The PALB2 Gene Fanconi Anemia Type N Genetic Test is a specialized diagnostic tool designed to identify mutations in the PALB2 gene, which are linked to the development of Fanconi anemia type N, a rare and inherited form of anemia that leads to decreased production of blood cells, increased risk of cancer, and other serious health problems. This test is crucial for individuals with a family history of the condition or those exhibiting symptoms, as early detection can significantly influence management and treatment strategies.

Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific mutations in the PALB2 gene. The accuracy and reliability of the test results from DNA Labs UAE make it a valuable resource for affected families and their healthcare providers.

The cost of the PALB2 Gene Fanconi Anemia Type N Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the test provides essential information for the genetic counseling process, guiding both preventative measures and therapeutic interventions for individuals at risk. This test represents a critical step towards personalized medicine, offering hope and options for those facing the challenges of Fanconi anemia type N.

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PALB2 Gene Fanconi Anemia Type N Genetic Test

Components:

  • Test Name: PALB2 Gene Fanconi Anemia Type N Genetic Test
  • 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 PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type N.

Test Details:

The PALB2 gene is associated with Fanconi anemia type N, which is a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the PALB2 gene and identify any mutations or variants that may be present.

NGS testing involves sequencing the DNA of an individual to identify any changes or abnormalities in the PALB2 gene. This type of testing can provide valuable information about the specific genetic variants that may be contributing to the development of Fanconi anemia type N. By identifying these genetic variants, healthcare professionals can better understand the underlying cause of the disease and develop personalized treatment plans for affected individuals.

NGS testing can also be used to provide genetic counseling and help with family planning decisions. It’s important to note that NGS testing may not be available in all healthcare settings, and it may require a referral to a specialized genetics laboratory. Additionally, the interpretation of NGS test results can be complex and should be done by a healthcare professional with expertise in genetics.

Overall, NGS genetic testing for the PALB2 gene can provide valuable information for the diagnosis, management, and genetic counseling of individuals with Fanconi anemia type N.

Test Name PALB2 Gene Fanconi anemia type N 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 PALB2 Gene Fanconi anemia type N NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Fanconi anemia type N
Test Details

The PALB2 gene is associated with Fanconi anemia type N, which is a rare genetic disorder characterized by bone marrow failure, developmental abnormalities, and an increased risk of cancer. NGS (Next-Generation Sequencing) genetic testing can be used to analyze the PALB2 gene and identify any mutations or variants that may be present.

NGS testing involves sequencing the DNA of an individual to identify any changes or abnormalities in the PALB2 gene. This type of testing can provide valuable information about the specific genetic variants that may be contributing to the development of Fanconi anemia type N.

By identifying these genetic variants, healthcare professionals can better understand the underlying cause of the disease and develop personalized treatment plans for affected individuals. NGS testing can also be used to provide genetic counseling and help with family planning decisions.

It’s important to note that NGS testing may not be available in all healthcare settings, and it may require a referral to a specialized genetics laboratory. Additionally, the interpretation of NGS test results can be complex and should be done by a healthcare professional with expertise in genetics.

Overall, NGS genetic testing for the PALB2 gene can provide valuable information for the diagnosis, management, and genetic counseling of individuals with Fanconi anemia type N.

SKU: TEST-2315 Category:

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