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Development of specific growth charts for children with Fanconi anemia
1 INTRODUCTION Fanconi anemia (FA) is a rare, autosomal recessive condition, estimated to occur in 1 in 130,000 live births (McReynolds et al., 2020). FA is characterized by a deficiency in DNA repair proteins that puts patients at risk of bone marrow failure at an early age and causes a later predisposition for cancer (Soulier, 2011).
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