Infantile osteopetrosis is a lethal disorder resulting from a severe defect
in the ability of osteoclasts to resorb bone. The only therapy shown to be
capable of providing lasting benefit is allogeneic hematopoietic stem cell
transplantation (HCT), We report the outcome of 10 patients with infantile
malignant osteopetrosis treated with HCT from an HLA A, B, DRB1 matched (n
= 6) or A or B locus mismatched (n = 4) family member or unrelated donor a
t the University of Minnesota between 1978 and 1997, Eight of 10 patients a
chieved primary engraftment; secondary graft failure was seen in two patien
ts. Five of 10 patients survive; three with full or partial donor chimerism
and two with autologous hematological recovery. Transient or partial donor
chimerism can be sufficient to correct the hematological manifestations of
osteopetrosis, We recommend early referral for consideration of HCT with a
related or unrelated donor as neurosensory manifestations of osteopetrosis
are generally not reversible. Donor engraftment may be easier to achieve e
arly in the course of the disease.