Progressive spastic paraparesis: Hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis

被引：38

作者：

Fink, JK

机构：

[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA

[2] Ann Arbor Vet Affairs Med Ctr, Geriatr Res Educ & Care Ctr, Ann Arbor, MI USA

来源：

SEMINARS IN NEUROLOGY | 2001年 / 21卷 / 02期

关键词：

hereditary spastic paraplegia; primary lateral sclerosis; amyotrophic lateral sclerosis; spinal cord disease; motor neuron disease; spastin; paraplegin;

D O I：

10.1055/s-2001-15265

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

The syndrome of insidiously progressive spastic weakness of both legs occurs in a number of etiologically distinct disorders including hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), and sometimes in amyotrophic lateral sclerosis (ALS), This review summarizes the clinical and pathologic relationship between these disorders.

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页码：199 / 207

页数：9

相关论文

共 68 条

[1]

Battistella PA, 1997, GIORN NEUROPSI EVOL, V17, P201

[2] STRUMPELLS FAMILIAL SPASTIC PARAPLEGIA - GENETICS AND NEUROPATHOLOGY [J].

BEHAN, WMH ;

MAIA, M .

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1974, 37 (01) :8-20

[3] MOTOR-NEURON DISEASE (AMYOTROPHIC-LATERAL-SCLEROSIS) ARISING FROM LONGSTANDING PRIMARY LATERAL SCLEROSIS [J].

BRUYN, RPM ;

KOELMAN, JHTM ;

TROOST, D ;

DEJONG, JMBV .

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 58 (06) :742-744

[4]

BUGE A, 1979, REV NEUROL, V135, P329

[5] Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance [J].

Byrne, PC ;

Webb, S ;

McSweeney, F ;

Burke, T ;

Hutchinson, M ;

Parfrey, NA .

EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 (03) :275-282

[6] Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia [J].

Cambi, F ;

Tang, XM ;

Cordray, P ;

Fain, PR ;

Keppen, LD ;

Barker, DF .

NEUROLOGY, 1996, 46 (04) :1112-1117

[7] Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease [J].

Casari, G ;

De Fusco, M ;

Ciarmatori, S ;

Zeviani, M ;

Mora, M ;

Fernandez, P ;

De Michele, G ;

Filla, A ;

Cocozza, S ;

Marconi, R ;

Dürr, A ;

Fontaine, B ;

Ballabio, A .

CELL, 1998, 93 (06) :973-983

[8]

CLAUS D, 1990, ANN NEUROL, V28, P43

[9] TROYER SYNDROME - A RECESSIVE FORM OF SPASTIC PARAPLEGIA WITH DISTAL MUSCLE WASTING [J].

CROSS, HE ;

MCKUSICK, VA .

ARCHIVES OF NEUROLOGY, 1967, 16 (05) :473-+

[10] A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3 [J].

De Michele, G ;

De Fusco, M ;

Cavalcanti, F ;

Filla, A ;

Marconi, R ;

Volpe, G ;

Monticelli, A ;

Ballabio, A ;

Casari, G ;

Cocozza, S .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :135-139

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