Conclusions A Chinese patients with psychomotor retardation, liver dysfunction, skeletal abnormality due to infantile GM1 gangliosidosis was reported. 结论本文报道了1例婴儿型GM1神经节苷脂沉积病,以智力运动落后为主,伴肝损害及骨骼异常。
Infantile type of GM_2 gangliosidosis 婴儿型GM2神经节苷脂沉积症
Studies on the molecular mechanism of GM_2 gangliosidosis GM2神经节苷脂沉积症发病的分子机理研究