REVERSAL OF EARLY NEUROLOGIC AND NEURORADIOLOGICAL MANIFESTATIONS OF X-LINKED ADRENOLEUKODYSTROPHY BY BONE-MARROW TRANSPLANTATION

被引:268
作者
AUBOURG, P
BLANCHE, S
JAMBAQUE, I
ROCCHICCIOLI, F
KALIFA, G
NAUDSAUDREAU, C
ROLLAND, MO
DEBRE, M
CHAUSSAIN, JL
GRISCELLI, C
FISCHER, A
BOUGNERES, PF
机构
[1] HOP ST VINCENT DE PAUL,DEPT PEDIAT ENDOCRINOL,F-75674 PARIS 14,FRANCE
[2] HOP ST VINCENT DE PAUL,DEPT PEDIAT NEUROL,F-75674 PARIS 14,FRANCE
[3] HOP ST VINCENT DE PAUL,DEPT PEDIAT RADIOL,F-75674 PARIS 14,FRANCE
[4] HOP ENFANTS MALAD,INSERM,U132,PARIS,FRANCE
[5] CTR HOSP,DEPT PEDIAT ENDOCRINOL,LORIENT,FRANCE
[6] HOP DEBROUSSE,DEPT BIOCHEM,F-69005 LYONS,FRANCE
关键词
D O I
10.1056/NEJM199006283222607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
X-LINKED adrenoleukodystrophy is an inherited peroxisomal disease caused by a defective gene located within the Xq28 region of the X chromosome.1 Childhood adrenoleukodystrophy is characterized by multifocal demyelination of the central nervous system and adrenal insufficiency.2 It is associated with an impairment of the degradation of saturated very-long-chain fatty acids.3 4 5 These fatty acids accumulate in the cholesterol ester and ganglioside fractions of the patients' white matter and adrenal cortex,2 as well as in plasma and red cells,6 providing biochemical clues to the diagnosis of the disease. Adrenoleukodystrophy has a wide phenotypic variation, but most cases appear in childhood or adolescence. © 1990, Massachusetts Medical Society. All rights reserved.
引用
收藏
页码:1860 / 1866
页数:7
相关论文
共 31 条
[1]   MRI DETECTS CEREBRAL INVOLVEMENT IN NEUROLOGICALLY ASYMPTOMATIC PATIENTS WITH ADRENOLEUKODYSTROPHY [J].
AUBOURG, P ;
SELLIER, N ;
CHAUSSAIN, JL ;
KALIFA, G .
NEUROLOGY, 1989, 39 (12) :1619-1621
[2]  
AUBOURG P, 1985, J LIPID RES, V26, P263
[3]   LINKAGE OF ADRENOLEUKODYSTROPHY TO A POLYMORPHIC DNA PROBE [J].
AUBOURG, PR ;
SACK, GH ;
MEYERS, DA ;
LEASE, JJ ;
MOSER, HW .
ANNALS OF NEUROLOGY, 1987, 21 (04) :349-352
[4]  
BROWN FR, 1982, JOHNS HOPKINS MED J, V151, P164
[5]  
CARPENTER G G, 1984, Pediatric Research, V18, p374A, DOI 10.1203/00006450-198404001-01687
[6]   APHASIA WITH NON-HEMORRHAGIC LESIONS IN THE BASAL GANGLIA AND INTERNAL CAPSULE [J].
DAMASIO, AR ;
DAMASIO, H ;
RIZZO, M ;
VARNEY, N ;
GERSH, F .
ARCHIVES OF NEUROLOGY, 1982, 39 (01) :15-20
[7]  
DUCHEN L, 1980, NEUROLOGICAL MUTATIO, P107
[8]   PERIVASCULAR MICROGLIAL CELLS OF THE CNS ARE BONE-MARROW DERIVED AND PRESENT ANTIGEN INVIVO [J].
HICKEY, WF ;
KIMURA, H .
SCIENCE, 1988, 239 (4837) :290-292
[9]   BIOCHEMICAL-ABNORMALITIES IN RHIZOMELIC CHONDRODYSPLASIA PUNCTATA [J].
HOEFLER, G ;
HOEFLER, S ;
WATKINS, PA ;
CHEN, WW ;
MOSER, A ;
BALDWIN, V ;
MCGILLIVARY, B ;
CHARROW, J ;
FRIEDMAN, JM ;
RUTLEDGE, L ;
HASHIMOTO, T ;
MOSER, HW .
JOURNAL OF PEDIATRICS, 1988, 112 (05) :726-733
[10]   DONOR-DERIVED CELLS IN THE CENTRAL NERVOUS-SYSTEM OF TWITCHER MICE AFTER BONE-MARROW TRANSPLANTATION [J].
HOOGERBRUGGE, PM ;
SUZUKI, K ;
SUZUKI, K ;
POORTHUIS, BJHM ;
KOBAYASHI, T ;
WAGEMAKER, G ;
VANBEKKUM, DW .
SCIENCE, 1988, 239 (4843) :1035-1038