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GTR Home > Tests > Fanconi Anemia Panel

Overview

Test name

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Fanconi Anemia Panel

Purpose of the test

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This is a clinical test intended for Help: Diagnosis

Condition

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How to order

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Complete the appropriate test requisiton and have it signed by the referring physician.
Order URL Help: http://www.cincinnatichildrens.org/service/d/diagnostic-labs/molecular-genetics/requisition/

Methodology

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Molecular Genetics
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

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Clinical utility

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Not provided

Clinical validity

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Not provided

Testing strategy

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Chromosome breakage and complementation testing can be ordered sequentially along with molecular genetic testing. Single-gene testing is also available for the genes on this panel, with the exception of FANCD1. 000 Complete the appropriate test requisiton and have it signed by the referring physician.

Suggested reading

Practice guidelines

  • FARF, 2020
    Fanconi Anemia Clinical Care Guidelines, Fifth Edition.
  • FARF, 2008
    Fanconi Anemia Research Fund, Guidelines for Diagnosis and Management, 2008 (See 2020 Update)

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.