Examining 61 youths diagnosed with sickle cell syndromes, this study f
ocused on both protective and risk factors of adaptive behavioral func
tioning in these children. Demographic characteristics (age, sex, inte
lligence, and socioeconomic status), severity of disease (number of da
ys hospitalized, emergency room visits, hemoglobin, and school days mi
ssed), behavioral adjustment, and family functioning were examined to
determine their relation to adaptive behavioral competencies. Age, sex
, and intellectual functioning were found to be efficient predictors o
f the majority of adaptive behavioral domains, with higher adaptive fu
nctioning being associated with younger children, girls, and greater i
ntellectual functioning. Adjustment difficulties characterized by inte
rnalizing symptoms were found to predict communication and global adap
tive functioning. Within the context of a risk-resistance adaptation m
odel, the present data were interpreted to support the use of secondar
y prevention efforts for children with sickle cell syndrome who may be
designated at high risk for developmental delays.