Clinical, Cytogenetic and Molecular Insights from 32 Years of the Portuguese Fanconi Anemia Cohort

Fanconi anemia (FA) is a rare monogenic chromosome breakage syndrome that presents variable morphologic abnormalities and progressive bone marrow failure. Based on over 30 years of diagnostic experience, our main goal was to describe the Portuguese FA population and assess potential clinical/analytical phenotypic correlations with both molecular variants and chromosome instability (CI).