Fanconi anemia (FA) is a rare genetic condition associated with pathogenic variants of several genes involved in DNA repair. Clinically, FA can present at birth with multiple congenital anomalies and growth restriction, and progresses over time with bone marrow failure and increased risk of malignancy. The average age of onset of bone marrow failure is 7.6 years, with a cumulative probability of occurrence of 90% by age 40 years. 1 The risk of developing
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