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Clinical pictures of 2 cases with I-cell disease patients, 8 and 11 months old female, were analyzed.
Characteristic coarse facial features, gum hypertrophy, retarded growth and dysostosis multiplex
were observed in both cases. Under phase contrast microscopic examination, cultured fibroblasts of
skin of case I patient had their cytoplasm filled with numerous dark granules leaving only a
juxtanuclear crescent free of inclusions. We report... |
