TREATMENT OF LATE INFANTILE METACHROMATIC LEUKODYSTROPHY BY BONE-MARROW TRANSPLANTATION

被引:113
作者
KRIVIT, W
SHAPIRO, E
KENNEDY, W
LIPTON, M
LOCKMAN, L
SMITH, S
SUMMERS, CG
WENGER, DA
TSAI, MY
RAMSAY, NKC
KERSEY, JH
YAO, JK
KAYE, E
机构
[1] UNIV MINNESOTA,DEPT PEDIAT,BONE MARROW TRANSPLANT PROGRAM,MINNEAPOLIS,MN 55455
[2] UNIV MINNESOTA,DIV PEDIAT NEUROL,MINNEAPOLIS,MN 55455
[3] UNIV MINNESOTA,DEPT OPHTHALMOL,MINNEAPOLIS,MN 55455
[4] UNIV MINNESOTA,DEPT LAB MED & PATHOL,MINNEAPOLIS,MN 55455
[5] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT MED GENET,PHILADELPHIA,PA 19107
[6] DEPT VET AFFAIRS,PITTSBURGH,PA
[7] NEW ENGLAND MED CTR,BOSTON,MA 02111
关键词
D O I
10.1056/NEJM199001043220106
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
METACHROMATIC leukodystrophy of the late infantile type, an autosomal recessive inherited disorder caused by a deficiency of arylsulfatase A activity, is characterized by progressive mental regression, loss of speech, quadriparesis, peripheral neuropathy, and death within a few years of onset.1 We describe a 10-year-old girl with metachromatic leukodystrophy in whom neurophysiologic function and sulfatide metabolism had improved after she received a bone marrow transplant five years before. These results may encourage the use of bone marrow transplantation in other patients with metachromatic leukodystrophy early in the course of the disease, when the degree of central nervous system impairment and the. © 1990, Massachusetts Medical Society. All rights reserved.
引用
收藏
页码:28 / 32
页数:5
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