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13号染色体综合征中的浦肯野细胞包涵体和“脑发育不全”

Purkinje cell inclusions and 'atelencephaly' in 13q-chromosomal syndrome.

作者信息

Towfighi J, Ladda R L, Sharkey F E

出版信息

Arch Pathol Lab Med. 1987 Feb;111(2):146-50.

PMID:3028313
Abstract

Severe microcephaly was present from birth in a child with a 13q-chromosomal syndrome [46,XY,del(13)(q22q31)]. He died at 20 months of age. Neuropathologic findings included atelencephaly and eosinophilic cytoplasmic inclusions in cerebellar Purkinje cells. Ultrastructurally, the inclusions consisted of stacks of parallel cisternae separated by electron-dense granular material. The relationship between these inclusions and the smaller cytoplasmic inclusions known as "lamellar bodies" is discussed, and the central nervous system malformations in this syndrome are reviewed.

摘要

一名患有13号染色体综合征[46,XY,del(13)(q22q31)]的儿童自出生就存在严重小头畸形。他在20个月大时死亡。神经病理学检查结果包括脑发育不全以及小脑浦肯野细胞中的嗜酸性细胞质包涵体。在超微结构上,这些包涵体由被电子致密颗粒物质分隔的平行扁平囊堆叠组成。本文讨论了这些包涵体与被称为“板层小体”的较小细胞质包涵体之间的关系,并对该综合征中的中枢神经系统畸形进行了综述。

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