Bone marrow failure in children may result from congenital or acquired dise
ases. Regardless of the etiology, prognosis depends upon the severity of im
pairment of hematopoiesis. With supportive care alone, 80% of patients with
acquired severe marrow failure used to die of bleeding, infection or other
complications (Camitta et al., 1976, Blood, 48, 63-70). Recently, both bon
e marrow transplantation, granulocyte colony stimulating factors and immuno
suppression have greatly improved the outcome of children with marrow failu
re. This paper reviews the current status of bone marrow transplantation fo
r the treatment of children with severe aplastic anemia and related disorde
rs. Recommendations are made regarding the optimal timing of marrow transpl
antation in regard to the severity of disease and the availability of a rel
ated or unrelated marrow donor.