About Fanconi Anaemia

What is Fanconi Anaemia?

FA is a rare, cancer-predisposing disorder affecting about 150 or more families in the UK (the true extent is unknown) manifested by:

There are 13 genetic subgroups, also known as complementation groups, reflecting 13 different proteins that can be potentially affected in the Fanconi pathway, a DNA housekeeping mechanism.

Some of these genetic subgroups have additional issues such as subgroup FA-D1, where affected children are at high risk of brain medulloblastoma and renal Wilm’s tumour. Some FA genetic subgroup carriers are also at increased risk of malignancy. BRCA2, one of the ‘breast cancer genes’ is actually part of the Fanconi pathway. A FA-D1 affected child is where both parents are carrier for BRCA2 with resultant increased breast cancer risk for the mother.

The UK and Ireland Fanconi Anaemia Clinical Network’s Standards of Care document provides information aimed at doctors and clinicians. Copies are also available in hard copy on request either for you or for your doctor or consultant. As the condition is very rare, knowledge in the medical profession is scant. The Standards of Care document  was produced to ensure consistency of patient care across the UK and Ireland.

The US Fanconi Anaemia Research Fund Fact Sheet gives a good overview of the condition. Their handbook entitled Fanconi Anemia: A Handbook for Families and their Physicians is currently under revision and not available.

The ‘Contact a Family’ website has some UK-based information written by Dr C G Steward, Reader in Stem Cell Research, Bristol Children’s Hospital, Bristol, UK.

Further Sources of  Information on Fanconi Anaemia

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