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铜-组氨酸疗法治疗门克斯病。

Copper-histidine therapy for Menkes disease.

作者信息

Sarkar B, Lingertat-Walsh K, Clarke J T

机构信息

Department of Biochemistry, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

J Pediatr. 1993 Nov;123(5):828-30. doi: 10.1016/s0022-3476(05)80870-4.

Abstract

Menkes disease is an X-linked genetic disorder of copper transport that results in death from severe progressive neurodegeneration by the age of 3 years. We report here our 17 years' experience with the treatment of Menkes disease with subcutaneous administration of copper-histidine. Two patients (16 and 6 years of age) whose therapy was begun within 1 month of birth have done well neurologically. The other five patients have done poorly despite treatment initiated at 2 to 7 months of age. Copper-histidine therapy may be an effective treatment if started early.

摘要

门克斯病是一种X连锁的铜转运基因障碍疾病,会导致严重进行性神经退行性变,患者通常在3岁前死亡。我们在此报告了17年来皮下注射组氨酸铜治疗门克斯病的经验。两名在出生后1个月内开始治疗的患者(分别为16岁和6岁),神经功能状况良好。另外五名患者尽管在2至7个月大时开始治疗,但效果不佳。如果早期开始治疗,组氨酸铜疗法可能是一种有效的治疗方法。

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