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The differential diagnosis of adult onset metachromatic leukodystrophy and early onset familial Alzheimer disease in an Alzheimer clinic population.

作者信息

Sadovnick A D, Tuokko H, Applegarth D A, Toone J R, Hadjistavropoulos T, Beattie B L

机构信息

Department of Medical Genetics, University of British Columbia, Vancouver.

出版信息

Can J Neurol Sci. 1993 Nov;20(4):312-8. doi: 10.1017/s031716710004823x.

DOI:10.1017/s031716710004823x
PMID:8313247
Abstract

Clinical differentiation between forms of progressive dementia can prove difficult, particularly when relatively rare forms of dementia are involved. Factors such as family history of dementia, age at onset, presenting features such as personality change, cognitive deficits, psychiatric symptoms, and clinical course (progressive deterioration; retention of skills over time) may prove useful for directing investigations to identify underlying pathology and genetic implications. This is illustrated by two patient reports. Each patient had the onset of memory/behavioral problems at approximately age 40 years, was initially given a psychiatric, non-dementing diagnosis, and had a positive family history for early onset behavioral and memory problems. After longitudinal assessment, the diagnosis of Alzheimer disease was confirmed at autopsy in one patient and a diagnosis of familial, adult-onset metachromatic leukodystrophy in the other.

摘要

相似文献

1
The differential diagnosis of adult onset metachromatic leukodystrophy and early onset familial Alzheimer disease in an Alzheimer clinic population.
Can J Neurol Sci. 1993 Nov;20(4):312-8. doi: 10.1017/s031716710004823x.
2
Late-Onset Metachromatic Leukodystrophy with Early Onset Dementia Associated with a Novel Missense Mutation in the Arylsulfatase A Gene.迟发性异染性脑白质营养不良伴早发性痴呆与芳基硫酸酯酶A基因新错义突变相关
J Alzheimers Dis. 2016;51(3):683-7. doi: 10.3233/JAD-150819.
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[Neuropathy in adult metachromatic leukodystrophy].[成人异染性脑白质营养不良中的神经病变]
Ugeskr Laeger. 1994 Apr 11;156(15):2252-3.
4
Early thalamic and cortical hypometabolism in adult-onset dementia due to metachromatic leukodystrophy.
Acta Neurol Belg. 1999 Sep;99(3):185-8.
5
Characteristics of the dementia in late-onset metachromatic leukodystrophy.
Neurology. 1994 Apr;44(4):662-5. doi: 10.1212/wnl.44.4.662.
6
Adult metachromatic leukodystrophy. Value of computed tomographic scanning and magnetic resonance imaging of the brain.成人异染性脑白质营养不良。脑部计算机断层扫描和磁共振成像的价值。
Arch Neurol. 1987 Feb;44(2):225-7. doi: 10.1001/archneur.1987.00520140083022.
7
[Adult form of metachromatic leukodystrophy with predominantly psychotic manifestations].
Nervenarzt. 1992 Jul;63(7):444-6.
8
[Metachromatic leukodystrophy: an exceptional cause of dementia in the adult].
Neurologia. 1992 May;7(5):114-6.
9
[Metachromatic leukodystrophy simulating schizophrenia-like psychosis].[模拟精神分裂症样精神病的异染性脑白质营养不良]
Nervenarzt. 1997 Sep;68(9):754-8. doi: 10.1007/s001150050191.
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Neuropsychological deficits in obligatory heterozygotes for metachromatic leukodystrophy.异染性脑白质营养不良的 obligatory 杂合子中的神经心理学缺陷 。 注:这里“obligatory”不太明确具体准确意思,可能是特定医学语境下有特殊含义的术语,常规理解为“强制的、必须的”等意思,在医学文献中可能有更专业的指代。
Hum Genet. 1988 May;79(1):8-12. doi: 10.1007/BF00291701.

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Metachromatic leukodystrophy: a case of triplets with the late infantile variant and a systematic review of the literature.异染性脑白质营养不良:一例三胞胎患晚发性婴儿型变异型病例及文献系统综述
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Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A gene.
加拿大新斯科舍省三个家族中的异染性脑白质营养不良:芳基硫酸酯酶A基因中的一个反复出现的突变。
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