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

[61]

2-O

[62] MULTISYSTEM INVOLVEMENT OF THE CENTRAL-NERVOUS-SYSTEM IN STRUMPELLS DISEASE - A NEUROPHYSIOLOGICAL AND NEUROPSYCHOLOGICAL STUDY [J].

TEDESCHI, G ;

ALLOCCA, S ;

DICOSTANZO, A ;

CARLOMAGNO, S ;

MERLA, F ;

PETRETTA, V ;

TORIELLO, A ;

TRANCHINO, G ;

AMBROSIO, G ;

BONAVITA, V .

JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 103 (01) :55-60

[63] STRUMPELL FAMILIAL SPASTIC PARAPLEGIA - AN ELECTROPHYSIOLOGICAL DEMONSTRATION OF SELECTIVE CENTRAL DISTAL AXONOPATHY [J].

UNCINI, A ;

TREVISO, M ;

BASCIANI, M ;

GAMBI, D .

ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1987, 66 (02) :132-136

[64] A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28 [J].

Vazza, G ;

Zortea, M ;

Boaretto, F ;

Micaglio, GF ;

Sartori, V ;

Mostacciuolo, ML .

AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) :504-509

[65] Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p [J].

Webb, S ;

Coleman, D ;

Byrne, P ;

Parfrey, N ;

Burke, T ;

Hutchinson, J ;

Hutchinson, M .

BRAIN, 1998, 121 :601-609

[66] Two families with autosomal recessive spastic paraplegia, pigmented maculopathy, and dementia [J].

Webb, S ;

Patterson, V ;

Hutchinson, M .

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1997, 63 (05) :628-632

[67] Pelizaeus-Merzbacher disease: Identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH [J].

Woodward, K ;

Kendall, E ;

Vetrie, D ;

Malcolm, S .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :207-217

[68] PRIMARY LATERAL SCLEROSIS - A CLINICAL-DIAGNOSIS REEMERGES [J].

YOUNGER, DS ;

CHOU, S ;

HAYS, AP ;

LANGE, DJ ;

EMERSON, R ;

BRIN, M ;

THOMPSON, H ;

ROWLAND, LP .

ARCHIVES OF NEUROLOGY, 1988, 45 (12) :1304-1307

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