CNS ABNORMALITIES IN PATIENTS WITH FAMILIAL AMYLOIDOSIS, FINNISH TYPE (FAF)

被引:10
作者
KIURU, S [1 ]
SEPPALAINEN, AM [1 ]
SALONEN, O [1 ]
HOKKANEN, L [1 ]
SOMER, H [1 ]
PALO, J [1 ]
机构
[1] UNIV HELSINKI, DEPT RADIOL, SF-00290 HELSINKI, FINLAND
来源
AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION | 1995年 / 2卷 / 01期
关键词
AMYLOIDOSIS; GELSOLIN; CENTRAL NERVOUS SYSTEM (CNS); FAMILIAL AMYLOID POLYNEUROPATHY (FAP); EVOKED POTENTIAL (EP); NEUROPSYCHOLOGY; MAGNETIC RESONANCE IMAGING (MRI);
D O I
10.3109/13506129509031884
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thirty-one patients with familial amyloidosis, Finnish (FAF) or Agel amyloidosis were studied for signs of central nervous system (CNS) involvement. Clinical neurological examination, conventional cerebrospinal fluid (CSF) studies and computed tomographic (CT) scanning findings were largely normal. In magnetic resonance imaging (MRI), punctate leukoencephalopathy (p<0.05), mostly frontal, and periventricular (p<0.05) and intrapontine signal hyperintensities (p<0.05) were more common in patients than in age-marched control subjects. In comparison with age-matched control subjects, the patients had prolonged central conduction in somatosensory evoked potentials (SEPs) (p<0.05), prolonged brain stem auditory evoked potentials (BAEPs) (p<0.05), and delayed P100 in pattern reversal visual evoked potentials (PVEPs) (p<0.0001). In addition, FAF patients showed mainly non-verbal abnormalities without dementia in neuropsychological testing. The results suggest minor, previously unrecognized CNS involvement in FAF.
引用
收藏
页码:22 / 30
页数:9
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