QJM, Vol 91, Issue 7 483-488, Copyright © 1998 by Oxford University Press
D Elstein, A Abrahamov, I Hadas-Halpern, A Meyer and A Zimran
The issue of the interplay of optimal dosage and frequency regimens for
enzyme replacement therapy in type I Gaucher disease has been a source of
controversy during the 7 years since the introduction of the
placenta-derived enzymatic preparation in 1991. We present the results of
treatment with the human recombinant form of the enzyme in 28 type I
Gaucher patients, who have been treated for 6 to 24 months. As long as cost
is an important factor in the management of patients with Gaucher disease,
low-dose low-frequency imiglucerase promises satisfactory clinical
improvement without compromising quality of life.
ORIGINAL PAPERS
Low-dose low-frequency imiglucerase as a starting regimen of enzyme replacement therapy for patients with type I Gaucher disease
Gaucher Clinic, Shaare-Zedek Medical Center, Jerusalem, Israel.
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