Literature DB >> 3028313

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

J Towfighi, R L Ladda, F E Sharkey.   

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.

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Year:  1987        PMID: 3028313

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  3 in total

1.  Novel eosinophilic inclusion in astrocytes.

Authors:  H Abe; S Yagishita; K Itoh; S Hamano
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  Ultrastructure of cerebellar capillary hemangioblastoma. VI. Concentric lamellar bodies of endoplasmic reticulum in stromal cells.

Authors:  K L Ho
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

3.  Aprosencephaly: review of the literature and report of a case with cerebellar hypoplasia, pigmented epithelial cyst and Rathke's cleft cyst.

Authors:  T S Kim; S Cho; D W Dickson
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

  3 in total

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