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Objective: To determine the prevalence, duration, and a potential cause of hum oral defect(s) in children with acute lymphoblastic leukemia (ALL) at least 1 ye ar after completion of chemotherapy. Study design: Antibody titers for mumps, ru beola, rubella, tetanus and diptheria toxoid, poliovirus serotypes 1, 2,and 3, H aemophilus influenzae type b, varicella, and hepatitis B were obtained from 100 children with ALL. Children with non-protective titers to these microbial antig ens were revaccinated and re-studied after anamnestic vaccine challenge. Result s: The percent of children with ALL wrotection.
Objective: To determine the prevalence, duration, and potential cause of hum oral defect (s) in children with acute lymphoblastic leukemia (ALL) at least 1 ye ar after completion of chemotherapy. Study design: Antibody titers for mumps, ru beola, rubella, tetanus and diptheria toxoid, poliovirus serotypes 1, 2, and 3, H aemophilus influenzae type b, varicella, and hepatitis B were obtained from 100 children with ALL. Children with non-protective titers to these microbial anti-graft were revaccinated and re -studied after anamnestic vaccine challenge. Result s: The percent of children with ALL wrote section.