Aurora Sheboygan Prices – Fanconi Anemia Complementation Group C Gene Analysis Costs $300

The Fanconi Anemia Complementation Group C (FANCC) Gene Analysis is a specialized genetic test offered at Aurora Medical Center Sheboygan County for $300. This test is used to detect mutations in the FANCC gene, which are associated with Fanconi anemia—a rare inherited disorder that can cause bone marrow failure and increase cancer risk. The $300 fee typically covers specimen collection (often a blood sample), laboratory processing, and genetic analysis. When considering this test, patients are advised to request an itemized estimate to clarify what is included, check if interpretation or follow-up genetic counseling is extra, and confirm insurance coverage or available payment plans.

Cost Breakdown

• Specimen collection (usually blood draw)
• Laboratory processing and DNA extraction
• FANCC gene sequencing and analysis
• Basic reporting of results to the ordering provider

Associated Costs

• Genetic counseling (before or after testing): often billed separately
• Follow-up appointments to discuss results
• Further genetic or diagnostic tests if mutations are detected
• Repeat testing for family members if familial mutations are found

Insurance & Payment Advice

• Contact your insurance provider before testing to ask if the FANCC gene analysis is covered, especially if you have a family history or related symptoms.
• Request a pre-authorization if necessary to avoid unexpected charges.
• Ask the billing office if financial assistance or payment plans are available if insurance does not cover the test.

Frequently Asked Questions

• What is the FANCC Gene Analysis used for?
  The FANCC Gene Analysis is used to detect mutations in the FANCC gene associated with Fanconi anemia, aiding in diagnosis and management of this genetic disorder.
• Who should consider this test?
  Individuals with a family history of Fanconi anemia or suggestive symptoms such as unexplained bone marrow failure or certain birth defects may benefit from this test.
• How is the test performed?
  The test is usually performed using a blood sample, which is analyzed in a specialized laboratory for changes in the FANCC gene.
• Is genetic counseling included in the $300 fee?
  Genetic counseling is typically not included and may be billed separately. Confirm with the provider before testing.
• Will insurance cover the cost?
  Coverage varies by insurance plan and medical necessity. Check with your insurer and ask your provider to help with any required documentation.
• What happens if a mutation is found?
  If a mutation is detected, your healthcare provider may recommend further testing, genetic counseling, or monitoring for Fanconi anemia symptoms.
• Are there risks or side effects from the test?
  The test itself involves a standard blood draw, which has minimal risk such as mild discomfort or bruising at the puncture site.
• How long does it take to get results?
  Results are typically available in a few weeks, depending on laboratory processing times.
• Will family members need to be tested?
  If a mutation is found, genetic testing may be recommended for close relatives to assess their risk.
• Can I pay for the test out of pocket?
  Yes, you can pay the $300 fee directly if insurance does not cover the test. Ask about payment options if needed.
• What should I do to prepare for the test?
  Usually, no special preparation is needed. Your provider will give you instructions if any are required.

Aurora Medical Center Sheboygan County offers a specialized genetic test known as the Fanconi Anemia Complementation Group C (FANCC) Gene Analysis, which is priced at $300. This test is designed to identify mutations in the FANCC gene, which are associated with Fanconi anemia, a rare genetic disorder that can lead to bone marrow failure and increased cancer risk. By analyzing the FANCC gene, healthcare providers can better understand a patient’s genetic predisposition to this condition, aiding in diagnosis and informing treatment decisions. The cost of $300 reflects the resources and expertise required to conduct this precise and potentially life-saving analysis.

What is the purpose of the FANCC Gene Analysis? – The FANCC Gene Analysis aims to detect mutations in the FANCC gene that are linked to Fanconi anemia, helping in the diagnosis and management of this genetic disorder.

Who should consider getting the FANCC Gene Analysis? – Individuals with a family history of Fanconi anemia or related symptoms may consider this test to assess their genetic risk.

How is the FANCC Gene Analysis performed? – The analysis is typically conducted using a blood sample, which is then examined in a laboratory to identify any mutations in the FANCC gene.

What are the implications of a positive FANCC Gene Analysis result? – A positive result indicates the presence of mutations associated with Fanconi anemia, which may require further medical evaluation and monitoring.

Is the FANCC Gene Analysis covered by insurance? – Coverage for genetic testing varies by insurance provider, so it is advisable to check with your insurer regarding the specifics of your plan.

How long does it take to receive results from the FANCC Gene Analysis? – The turnaround time for results can vary, but it generally takes a few weeks for the laboratory to process and analyze the sample.

Can the FANCC Gene Analysis predict the severity of Fanconi anemia? – While the test can identify mutations, it cannot predict the severity or specific symptoms of Fanconi anemia in an individual.

Are there any risks associated with the FANCC Gene Analysis? – The test itself poses minimal risk, typically involving only a standard blood draw, but there may be psychological implications of learning one’s genetic status.