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Levodopa-responsive parkinsonism in hereditary spastic paraplegia with thin corpus callosum.

Abstract：

:Hereditary spastic paraplegia with thin corpus callosum is a rare degenerative disease, which is characterized by a progressive weakness of the lower limbs with a hypoplastic corpus callosum, and is often associated with other symptoms such as mental impairment, amyotrophy, sensory disturbances, dysuria, nystagmus and cataract. We describe two siblings (brother and sister) who showed a thin corpus callosum on MRI, one of whom showed the pure form of progressive spastic paraplegia, while the other showed predominant levodopa-responsive parkinsonism. The present cases are illustrative of a phenotypic heterogeneity in the same family of spastic paraplegia with a thin corpus callosum, despite the identical neuroimaging findings, and also presented another form of autosomal recessive juvenile levodopa-responsive parkinsonism.

journal_name

Parkinsonism Relat Disord

journal_title

Parkinsonism & related disorders

authors

Kang SY,Lee MH,Lee SK,Sohn YH

doi

10.1016/j.parkreldis.2004.05.003

subject

Has Abstract

pub_date

2004-10-01 00:00:00

pages

425-7

issue

7

eissn

1353-8020

issn

1873-5126

pii

S1353802004000884

journal_volume

10

pub_type

杂志文章

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