Fanconi anemia (FA) is a rare congenital disease that is associated with progressive bone marrow failure, malformations and a significantly increased risk of cancer. The extent of the clinical manifestations of the disease, which is caused by at least 16 genes, varies considerably. The FA Registry was established to investigate the genetic causes and modifying factors and to better understand the natural history of the disease. We also aim to advise physicians and affected individuals and provide them with up-to-date information about the syndrome.
Prof. Dr. Dr. Christian Kratz is the head of the registry. The registry can also be used for consultation by medical professionals who care for patients with FA.
To the separate website of the Fanconi Anemia Registry
All further information, such as the documents required for registration, can be found on the separate website of the FA Register.
Contact persons and contact
| Function | Name of |
|---|---|
| Contact person | Beatrice Hoffmann Birte Sänger |
| Contact via | phone number |
|---|---|
| Telephone | +49 511 532-9408 |
| Fax | +49 511 532-161026 |
| FA-GPOH1@mh-hannover.de |