Related Experiment Videos
[Gaucher's disease: study of a family from Friuli]
L Virgolini1, F Silvestri, C Savignano
1Istituto di Morfologia Clinica e Sperimentale, Università degli Studi di Udine.
Minerva Medica
|March 1, 1993
Abstract:
Gaucher's disease is the most frequent of lysosomal storage diseases. In a family study two affected sisters of a type I patient were identified. Two of them underwent splenectomy, so reaching hematological normalization.