We have recently described a chemotactic defect in severely afflicted Gaucher disease patients. Two of the patients were treated with low-dose intravenous enzyme replacement (Ceredase). Marked improvement in their hematological status, organomegaly, and growth was observed. In addition, their chemotactic defect and their tendency towards infections were corrected within 1 year of treatment.
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Univ Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, Brazil
Doneda, D.
Mittelstadt, S. D.
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Univ Fed Rio Grande do Sul, Sch Med, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, Brazil
Mittelstadt, S. D.
Vairo, F. P.
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Hosp Clin Porto Alegre, Div Med Genet, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, Brazil
Vairo, F. P.
Netto, C. B.
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Hosp Clin Porto Alegre, Div Med Genet, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, Brazil
Netto, C. B.
Schwartz, I. V. D.
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Univ Fed Rio Grande do Sul, Postgrad Program Med Med Sci, Porto Alegre, RS, Brazil
Univ Fed Rio Grande do Sul, Dept Genet, Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Sch Med, LTD Lab, Porto Alegre, RS, Brazil