PROTRACTED FORM OF JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS

被引：31

作者：

GOEBEL, HH

PILZ, H

GULLOTTA, F

机构：

[1] UNIV GOTTINGEN, DIV NEUROPATHOL, D-3400 GOTTINGEN, FED REP GER

[2] UNIV GOTTINGEN, DEPT NEUROL, D-3400 GOTTINGEN, FED REP GER

[3] UNIV BONN, DIV NEUROPATHOL, D-5300 BONN 1, FED REP GER

来源：

ACTA NEUROPATHOLOGICA | 1976年 / 36卷 / 04期

关键词：

D O I：

10.1007/BF00699645

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Clinical and ultrastructural findings consisting of curvilinear and fingerprint residual bodies, in a protracted juvenile form of NCL were reported from a woman who died at the age of 35 yr. Homochrony and homotypy of her brother''s illness emphasized the intrafamilial similarities within subgroups of lysosomal disorders.

引用

页码：393 / 396

页数：4

共 11 条

[1] ELECTRON MICROSCOPY OF STORAGE CYTOSOMES IN KUFS DISEASE [J].