Erikson A, Aström M, Månsson J E
Department of Pediatrics, County Hospital Boden, Sweden.
Neuropediatrics. 1995 Aug;26(4):203-7. doi: 10.1055/s-2007-979754.
We report our experience from enzyme infusion therapy of eight patients with the Norrbottnian type of Gaucher disease (type 3) aged 4 to 42 years. All patients responded with increased well-being, decreased liver and spleen size and normalized hematological parameters. The children caught up in growth. No further neurological deterioration occurred and there were some indications of neurological improvement. Circulating glucosylceramide concentrations seemed to be a possible parameter to monitor the dosage of infused enzyme. The circulating glucosylceramide levels responded better in non-splenectomized patients. Enzyme infusion therapy can be recommended in type 3 Gaucher disease.
我们报告了对8例年龄在4至42岁的诺尔伯顿型戈谢病(3型)患者进行酶输注治疗的经验。所有患者均表现出健康状况改善、肝脏和脾脏体积减小以及血液学参数正常化。儿童实现了追赶生长。未出现进一步的神经功能恶化,且有一些神经功能改善的迹象。循环中的葡糖神经酰胺浓度似乎是监测输注酶剂量的一个可能参数。在未行脾切除术的患者中,循环葡糖神经酰胺水平反应更好。酶输注治疗可推荐用于3型戈谢病。