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PALB2 Gene Fanconi Anemia Type N Genetic Test

Original price was: $700.Current price is: $500.

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The PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test is a comprehensive genetic analysis that detects mutations in the PALB2 gene associated with Fanconi anemia type N. This next-generation sequencing test provides crucial information about inherited bone marrow failure syndromes and cancer predisposition. Individuals with family history of Fanconi anemia, unexplained bone marrow failure, or congenital abnormalities should consider this test. Early detection enables proactive medical management and family planning decisions. The test costs $500 USD and provides results within 3-4 weeks using blood or DNA samples. Genetic counseling is recommended before testing to understand implications and create family pedigree charts.

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PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test

Comprehensive Genetic Testing for Fanconi Anemia Type N

The PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test represents a cutting-edge diagnostic approach for identifying mutations in the PALB2 gene, which plays a critical role in DNA repair mechanisms and cellular health. Fanconi anemia type N is a rare inherited disorder characterized by bone marrow failure, congenital abnormalities, and increased cancer susceptibility. This advanced genetic test utilizes next-generation sequencing technology to provide comprehensive analysis of the PALB2 gene, offering patients and healthcare providers valuable insights into genetic predisposition and disease management strategies.

What Does This Test Measure and Detect?

This sophisticated genetic test specifically targets and analyzes the PALB2 gene for pathogenic variants associated with Fanconi anemia type N. The test detects:

  • Point mutations, deletions, and insertions in the PALB2 gene
  • Known pathogenic variants linked to Fanconi anemia type N
  • Novel genetic variations that may impact protein function
  • Inheritance patterns of PALB2 mutations
  • Carrier status for family planning purposes

Who Should Consider This Genetic Test?

This test is particularly recommended for individuals exhibiting symptoms or having risk factors including:

  • Family history of Fanconi anemia or related bone marrow disorders
  • Unexplained bone marrow failure or aplastic anemia
  • Congenital physical abnormalities such as short stature, skin pigmentation changes, or skeletal malformations
  • Increased cancer susceptibility, especially childhood cancers
  • Developmental delays or growth retardation
  • Individuals planning pregnancy with family history of Fanconi anemia
  • Patients with unexplained hematological abnormalities

Significant Benefits of PALB2 Genetic Testing

Undergoing the PALB2 Gene Fanconi Anemia Type N test provides numerous advantages:

  • Early Disease Detection: Identify genetic predisposition before symptom onset
  • Personalized Medical Management: Tailor surveillance and treatment strategies
  • Family Planning Guidance: Make informed reproductive decisions
  • Cancer Risk Assessment: Understand increased susceptibility to specific cancers
  • Comprehensive Genetic Counseling: Receive expert guidance on test implications
  • Proactive Health Monitoring: Implement appropriate screening protocols

Understanding Your Test Results

Your PALB2 genetic test results will fall into one of several categories:

  • Positive Result: Indicates the presence of a pathogenic PALB2 mutation associated with Fanconi anemia type N. This result confirms diagnosis and enables targeted medical management.
  • Negative Result: No pathogenic PALB2 mutations detected, significantly reducing but not completely eliminating Fanconi anemia risk.
  • Variant of Uncertain Significance (VUS): Identifies genetic changes with unknown clinical implications requiring further evaluation.
  • Carrier Status: Identifies individuals who carry one copy of a PALB2 mutation but may not develop symptoms.

All results should be interpreted in consultation with a genetic counselor or healthcare provider who can explain implications for your health and family members.

Test Pricing and Details

Test Component Details
Test Name PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test
Discount Price $500 USD
Regular Price $700 USD
Turnaround Time 3 to 4 Weeks
Sample Type Blood, Extracted DNA, or One Drop Blood on FTA Card
Testing Method Next-Generation Sequencing (NGS) Technology

Nationwide Testing Availability

We have diagnostic branches conveniently located across the United States, serving major metropolitan areas including New York, Los Angeles, Chicago, Houston, Phoenix, Philadelphia, San Antonio, San Diego, Dallas, and San Jose. Our state-of-the-art facilities ensure consistent, high-quality testing standards nationwide.

Take Control of Your Genetic Health Today

Understanding your genetic predisposition to Fanconi anemia type N can significantly impact your health management and family planning decisions. Our comprehensive PALB2 genetic testing provides the clarity and confidence you need to make informed healthcare choices. With advanced NGS technology and expert genetic counseling support, we deliver accurate, reliable results you can trust.

Ready to schedule your PALB2 Gene Fanconi Anemia Type N NGS Genetic DNA Test? Contact our genetic specialists today at +1(267) 388-9828 to book your appointment or discuss testing options. Our team is available to answer your questions and guide you through the testing process with compassion and expertise.