Fanconi Anemia

Fanconi Anemia

About Fanconi Anemia

Fanconi anemia is a rare autosomal recessive disorder that is caused by inactivation of one of at least 22 genes. Products of those genes have important role in DNA reparation during DNA replication. This disease affects many parts of the body and the diagnosis is based on the presence of the symptoms, clinical exams and genetic testing.

Recommendations

Understanding your genetic makeup can provide valuable insight into your health and potential risks for your offspring. Results in this category describe whether you’re a carrier of rare diseases. These are very unlikely to affect you but being a carrier of a rare disease can pose a risk for your children, when both you and your partner are carriers. This knowledge can help you make informed decisions about your future, and potentially reduce the risk of passing on genetic conditions to the next generation

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Recommendations

Understanding your genetic makeup can provide valuable insight into your health and potential risks for your offspring. Results in this category describe whether you’re a carrier of rare diseases. These are very unlikely to affect you but being a carrier of a rare disease can pose a risk for your children, when both you and your partner are carriers. This knowledge can help you make informed decisions about your future, and potentially reduce the risk of passing on genetic conditions to the next generation

Sources

We are currently working on preparing a better list of references and studies. It will be ready soon!

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