This disease often manifests during early childhood, and is characterised, in the majority of cases, by gradual malfunction of the bone marrow. Fanconi anemia can also be associated with various malformations, which vary greatly in severity and number, and increase the susceptibility to some types of cancer. Fanconi syndrome is a very rare genetic condition that affects around 180 people in France.

ORPHA84 – Fanconi anemia

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Centre of reference coordinator / Centre of reference constituentCompetence centreAssociated centre Undefined
Speciality : Adult Pediatric