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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days for obtaining the report for the test Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS is typically 14-21 days. This timeframe includes the time required for sample processing, sequencing, data analysis, and final report generation.

What are the prerequisites for the test Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS

  • Completed Test Requisition Form
  • Family history of breast and/or ovarian cancer
  • Personal history of breast and/or ovarian cancer
  • Personal or family history of other cancers associated with HBOC syndrome
  • Documentation of a pathogenic mutation in a known HBOC gene in the family
  • Consultation with a genetic counselor or healthcare provider

What are the measure values for the test Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS

  • BRCA1 Gene Analysis: Detected/Not Detected
  • BRCA1 Gene Deletion/Duplication Analysis: Detected/Not Detected
  • BRCA2 Gene Analysis: Detected/Not Detected
  • BRCA2 Gene Deletion/Duplication Analysis: Detected/Not Detected
  • ATM Gene Analysis: Detected/Not Detected
  • BARD1 Gene Analysis: Detected/Not Detected
  • BRIP1 Gene Analysis: Detected/Not Detected
  • CDH1 Gene Analysis: Detected/Not Detected
  • CHEK2 Gene Analysis: Detected/Not Detected
  • NBN Gene Analysis: Detected/Not Detected
  • NF1 Gene Analysis: Detected/Not Detected
  • PTEN Gene Analysis: Detected/Not Detected
  • STK11 Gene Analysis: Detected/Not Detected
  • TP53 Gene Analysis: Detected/Not Detected

What does this test Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS identify?

Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS

This test identifies mutations in specific genes that are associated with Hereditary Breast & Ovarian Cancer Syndrome (HBOC). This syndrome is characterized by an increased risk of breast and ovarian cancer due to inherited mutations in certain genes.

The test uses Next Generation Sequencing (NGS) technology to analyze multiple genes simultaneously, providing a comprehensive evaluation of genetic risk factors for HBOC. The genes included in the panel typically include BRCA1, BRCA2, TP53, PTEN, and other genes known to be associated with hereditary breast and ovarian cancer.

Identifying mutations in these genes can help determine an individual's risk of developing breast or ovarian cancer, as well as guide personalized treatment and management strategies. This information can also be used for genetic counseling and family planning purposes.

Why is this test Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS taken?

Individuals may choose to undergo the Hereditary Breast & Ovarian Cancer Syndrome (HBOC) Extended Panel By NGS test for a variety of reasons:

  • To assess their risk of developing hereditary breast and ovarian cancer
  • To determine if they carry genetic mutations that increase their risk of developing these cancers
  • To make informed decisions about their healthcare and potential preventive measures
  • To understand their family history and potential genetic risks for themselves and their relatives
  • To receive personalized medical management and screening recommendations based on their genetic profile

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