Different tests are used to diagnose and differentiate IBMFS.
These include:
You should consider genetic testing if you or your family members meet one or more of the following criteria:
If a faulty gene is identified, it can help guide your options for treatment and management.
If you are currently asymptomatic, it can help guide relevant screening and blood tests to detect bone marrow failure or cancer at its earliest, most treatable stage.
Genetic testing to identify these faulty genes will allow for personalised treatment and management options.
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