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[Gaucher's disease type 1: apropos of 17 cases]
N Belmatoug1, M de Bandt, E Oksenhendler
1Service de médecine interne, CHU Bichat-Claude-Bernard, Paris.
La Revue De Medecine Interne
|January 1, 1993
Abstract:
Gaucher's disease is characterized by accumulation of glucocerebroside (caused by an autosomally inherited deficiency of glucocerebrosidase) in the cells of the reticuloendothelial system. We report the clinical, laboratory, radiologic features of 17 patients with type 1 Gaucher's disease.