Aurora Burlington Charges $785 for Cytogenetics Breakage Syndrome Procedure

Aurora Medical Center Burlington, located at 252 McHenry St, Burlington, WI, offers a specialized medical service known as the Cytogenetics Breakage Syndrome Procedure, priced at $785. This procedure involves the analysis of chromosomes to detect breakage syndromes, which are genetic disorders characterized by an increased tendency for chromosome breakage. These syndromes can lead to various health issues, including developmental delays and increased cancer risk. The procedure is crucial for diagnosing such conditions, allowing for early intervention and management strategies to improve patient outcomes. The cost of $785 reflects the complexity and specialized nature of the testing involved.

What is the Cytogenetics Breakage Syndrome Procedure? – The Cytogenetics Breakage Syndrome Procedure is a diagnostic test that analyzes chromosomes to identify genetic disorders characterized by increased chromosome breakage.

Why is the procedure important? – This procedure is vital for diagnosing breakage syndromes, which can lead to serious health issues, enabling early intervention and management.

How much does the procedure cost at Aurora Medical Center Burlington? – The procedure costs $785 at Aurora Medical Center Burlington.

What conditions can be diagnosed with this procedure? – Conditions such as Fanconi anemia and other genetic disorders that involve chromosome instability can be diagnosed with this procedure.

Is the procedure covered by insurance? – Coverage for the Cytogenetics Breakage Syndrome Procedure depends on individual insurance plans; patients should verify with their provider.

How is the procedure performed? – The procedure involves collecting a blood sample, which is then analyzed in a laboratory to assess chromosome structure and integrity.

How long does it take to get results? – The time to receive results can vary, but it typically takes a few weeks for the laboratory analysis to be completed.

Who should consider undergoing this procedure? – Individuals with a family history of genetic disorders or symptoms suggestive of chromosome breakage syndromes should consider this procedure.

What are the potential outcomes of the procedure? – The procedure can confirm the presence of a breakage syndrome, leading to appropriate medical management and genetic counseling.