LATE-ONSET GLOBOID-CELL LEUKODYSTROPHY - REPORT ON 7 NEW PATIENTS

被引：27

作者：

FIUMARA, A ^{[1
]}

PAVONE, L ^{[1
]}

SICILIANO, L ^{[1
]}

TINE, A ^{[1
]}

PARANO, E ^{[1
]}

INNICO, G ^{[1
]}

机构：

[1] UNIV CATANIA,PEDIAT CLIN 1,VIALE A DORIA 6,I-95125 CATANIA,ITALY

来源：

CHILDS NERVOUS SYSTEM | 1990年 / 6卷 / 04期

关键词：

β-Galactosyl-ceramidase I deficiency; Globoid-cell leukodystrophy; Krabbe's disease; Late-onset;

D O I：

10.1007/BF01850970

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

During the past 12 years, ten cases of globoidcell leukodystrophy (GLD) have been followed up: seven of these patients were affected by the late infantile form. The authors point out the clinical aspects and the course of these patients and stress the high frequency of this form of GLD in Sicily. © 1990 Springer-Verlag.

引用

页码：194 / 197

页数：4

共 5 条

[1]

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[3] LATE-ONSET GLOBOID-CELL LEUCODYSTROPHY (KRABBES DISEASE) - CLINICAL AND GENETIC DELINEATION OF 2 FORMS AND THEIR RELATION TO THE EARLY-INFANTILE FORM [J].

LOONEN, MCB ;

VANDIGGELEN, OP ;

JANSE, HC ;

KLEIJER, WJ ;

ARTS, WFM .

NEUROPEDIATRICS, 1985, 16 (03) :137-142

[4]

LYON G, 1987, 1987 M EUR FED CHILD

[5] GLOBOID CELL LEUKODYSTROPHY - ADDITIONAL DEFICIENCY OF PSYCHOSINE GALACTOSIDASE [J].

MIYATAKE, T ;

SUZUKI, K .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 48 (03) :538-&

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