HEREDITARY ESSENTIAL MYOCLONUS

被引：3

作者：

ZONDA, T

SZABO, E

机构：

来源：

HUMAN HEREDITY | 1979年 / 29卷 / 06期

关键词：

D O I：

10.1159/000153070

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

A new family with the rare condition of hereditary essential myoclonus (HEM) and the literature on HEM are presented. Some of these cases may previously have been reported under the title of Friedreich's paramyoclonus multiplex. The present family, which is number 13 in the literature and in which 9 members in 3 generations had this benign disorder, is described. The diagnostic criteria have been tabulated.

引用

页码：348 / 350

页数：3

共 16 条

[1] MYOCLONUS - CLINICAL SIGNIFICANCE AND AN APPROACH TO CLASSIFICATION [J].

AIGNER, BR ;

MULDER, DW .

ARCHIVES OF NEUROLOGY, 1960, 2 (JUN) :600-615

[2] ON THE GENETICS OF ESSENTIAL MYOCLONIAS [J].

BECKER, PE ;

WIESER, S .

HUMANGENETIK, 1964, 1 (01) :14-23

[3]

BECKER PE, 1966, HUMANGENETIK, V5, P157

[4]

BIEMOND A, 1963, Psychiatr Neurol Neurochir, V66, P270

[5] HEREDITARY ESSENTIAL MYOCLONUS [J].

DAUBE, JR ;

PETERS, HA .

ARCHIVES OF NEUROLOGY, 1966, 15 (06) :587-+

[6]

ELLIOTT FA, 1949, P ROY SOC MED, V42, P66

[7]

FELDMANN H, 1964, ARCH PSYCHIATR NERVE, V205, P184

[8]

FORD FR, 1952, DISEASES NERVOUS SYS

[9]

LINDEMULDER FG, 1933, J NERV MENT DIS, V77, P489

[10]

LITTLEJOHN W S, 1949, South Med J, V42, P404

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