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小头畸形伴特殊脱髓鞘,酷似佩利措伊斯-梅茨巴赫病。

Microcephaly with peculiar demyelination mimicking Pelizaeus-Merzbacher disease.

作者信息

Kamoshita S, Igarashi M, Kono R

出版信息

Acta Neuropathol. 1977 Sep 26;40(1):95-8. doi: 10.1007/BF00688579.

DOI:10.1007/BF00688579
PMID:562057
Abstract

The neuropathological studies of a 4-year old idiot with microcephaly revealed a striking demyelinating disease compatible with Pelizaeus-Merzbacher disease. The case seemed to be best classified as the patchy demyelination type, but the most unusual finding was a prominent vasculature in some demyelinated areas. Intrauterine hypoxia was proposed as a causative factor of this type of demyelinative lesions.

摘要

对一名患有小头畸形的4岁白痴进行的神经病理学研究显示,有一种与佩利措伊斯-梅茨巴赫病相符的显著脱髓鞘疾病。该病例似乎最好归类为斑片状脱髓鞘型,但最不寻常的发现是在一些脱髓鞘区域有明显的血管系统。宫内缺氧被认为是这类脱髓鞘病变的一个致病因素。

相似文献

1
Microcephaly with peculiar demyelination mimicking Pelizaeus-Merzbacher disease.小头畸形伴特殊脱髓鞘,酷似佩利措伊斯-梅茨巴赫病。
Acta Neuropathol. 1977 Sep 26;40(1):95-8. doi: 10.1007/BF00688579.
2
[Pelizaeus-Merzbacher disease].[佩利措伊斯-梅茨巴赫病]
Neuropatol Pol. 1973 Apr-Jun;11(5):143-52.
3
Peculiar dysmorphic syndrome with orthochromatic leucodystrophy. Discussion of its relationship with Cockayne's syndrome and Pelizaeus-Merzbacher's disease.伴有正染性脑白质营养不良的特殊畸形综合征。关于其与科凯恩综合征及佩利措伊斯-梅茨巴赫病关系的讨论。
Acta Neuropathol. 1971;18(3):224-33. doi: 10.1007/BF00685068.
4
[An adult case of classical Pelizaeus-Merzbacher disease--magnetic resonance images and neuropathological findings].
Rinsho Shinkeigaku. 1993 Feb;33(2):187-93.
5
Late-life cavitating dystrophy of the cerebral and cerebellar white matter. A form of sudanophil leucodystrophy.脑和小脑白质的晚发性空泡性营养不良。一种嗜苏丹性脑白质营养不良的形式。
Eur Neurol. 1972;7(1):79-94. doi: 10.1159/000114415.
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The Wiedemann-Rautenstrauch or neonatal progeroid syndrome. Neuropathological study of a case.维德曼-劳滕施劳赫综合征或新生儿早老综合征。1例神经病理学研究。
Neuropediatrics. 1984 Feb;15(1):43-8. doi: 10.1055/s-2008-1052339.
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Differentiation of dys- and demyelination using diffusional anisotropy.
Pediatr Neurol. 1997 Jan;16(1):63-6. doi: 10.1016/s0887-8994(96)00249-4.
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Pelizacus-Merzbacher disease. Transitional form between classical and co-natal (Seitelberger) type.
Acta Neuropathol. 1969;14(2):108-17. doi: 10.1007/BF00686347.
9
Neuro-ocular considerations in the Pelizaeus-Merzbacher syndrome. A clinicopathologic study.佩利措伊斯-梅茨巴赫综合征的神经眼科考量。一项临床病理研究。
Am J Ophthalmol. 1968 Dec;66(6):1143-51. doi: 10.1016/0002-9394(68)90825-8.
10
[ON THE DEGREE OF VARIATION IN PELIZAEUS-MERZBACHER DISEASE. (WITH A CONTRIBUTION TO FAMILIAL MULTIPLE SCLEROSIS)].[关于佩利措伊斯-梅茨巴赫病的变异程度。(对家族性多发性硬化症的一项贡献)]
Acta Neuropathol. 1963 Nov 5;3:87-107. doi: 10.1007/BF00687059.

本文引用的文献

1
STUDIES OF CEREBRAL LIPIDS IN A RELAPSING CASE OF CARBON MONOXIDE POISONING.一氧化碳中毒复发病例的脑脂质研究
Acta Neuropathol. 1963 Apr 2;3:371-7. doi: 10.1007/BF00685994.
2
Neuropathological problems posed by carbon monoxide poisoning and anoxia.一氧化碳中毒和缺氧引发的神经病理学问题。
Prog Brain Res. 1967;24:75-100. doi: 10.1016/S0079-6123(08)60182-X.
3
[The leukoencephalopathies caused by carbon monoxide poisoning. Study of sixteen anatomo-clinical observations].[一氧化碳中毒所致白质脑病。16例解剖临床观察研究]
Acta Neuropathol. 1966 Jul 7;6(4):327-48. doi: 10.1007/BF00688162.
4
Central pontine myelinolysis in childhood and adolescence.儿童及青少年时期的中央桥脑髓鞘溶解症
Arch Dis Child. 1969 Jun;44(235):342-50. doi: 10.1136/adc.44.235.342.
5
Subacute necrotizing encephalomyelopathy (LEIGH).亚急性坏死性脑脊髓病(利氏病)
Ergeb Inn Med Kinderheilkd. 1970;29:155-219. doi: 10.1007/978-3-642-95138-1_4.
6
[Familial progressive leukoencephalopathy with vascular proliferation. Its eventual relation to subacute necrotizing encephalopathy].
Acta Neuropathol. 1974;28(2):143-50. doi: 10.1007/BF00710323.
7
[The infantile form of sudanophil leukodystrophy with non-calcifying meningeal angiomatosis].[伴有非钙化性脑膜血管瘤病的婴儿型嗜苏丹性脑白质营养不良]
Acta Neurol Psychiatr Belg. 1967 Jun;67(6):463-74.
8
Central pontine myelinolysis and medullary myelinolysis.中央桥脑髓鞘溶解症和延髓髓鞘溶解症。
Arch Pathol Lab Med. 1976 May;100(5):246-52.