Fanconi anemia is a rare genetic disease in which essential DNA repair pathway genes are mutated, disrupting the DNA damage response. Patients with Fanconi anemia experience hematological ...

Fanconi anemia (FA) is a rare, inherited disease primarily affecting children. While the outcome for people with FA tends to be poor, researchers predict that newer molecular and gene therapies can ...

Fanconi anemia is a rare inherited condition that can cause bone marrow failure, physical abnormalities, and an increased risk of some cancers. Symptoms include tiredness, infections, easy bruising, ...

Fanconi anemia is a rare inherited condition that can affect the thumbs. Some people with the condition may be born with extra, missing, or misshapen thumbs. While Fanconi anemia does not affect the ...

MINNEAPOLIS/ST. PAUL (2/26/2024) — Published in the American Journal of Medical Genetics, a University of Minnesota Medical School study found that it is normal for children with Fanconi anemia to be ...

Mutations in FANCX appear to cause a lethal form of Fanconi anemia, a finding that sheds light on unexplained pregnancy loss and offers new avenues for genetic screening. Fanconi anemia is an ...

Fanconi anemia is an aggressive, life-threatening disorder. Most individuals living with this rare genetic condition, characterized by bone marrow failure and cancer predisposition, survive into ...

Fanconi anaemia (FA) is a rare inherited disorder characterised by genomic instability, progressive bone marrow failure, and a predisposition to malignancies. Haematopoietic stem cell transplantation ...

Fanconi anemia is an aggressive, life-threatening disorder. Most individuals living with this rare genetic condition, characterized by bone marrow failure and cancer predisposition, survive into ...