Literature DB >> 1718183

Cortical cytoarchitectural and immunohistochemical studies on Zellweger syndrome.

S Takashima1, F Chan, L E Becker, S Houdou, Y Suzuki.   

Abstract

In two cases of Zellweger syndrome, Golgi studies revealed an irregular neuronal arrangement, the presence of immature neurons, poor dendritic arborization and poor spine development, all of which suggest abnormal morphogenesis and delayed maturation. In immunohistochemical studies with antisera against human catalase, negative staining of neurons suggested a decrease of catalase due to defects of microperoxisomes, and positive staining of myelination glia only in the internal capsule may have been related to delayed myelination. Abnormal peroxisomal membrane or its related metabolites may cause a migration disorder in intrauterine development and myelination disturbance in perinatal maturation.

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Year:  1991        PMID: 1718183     DOI: 10.1016/s0387-7604(12)80022-2

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  3 in total

Review 1.  Neuropathology of peroxisomal diseases.

Authors:  J J Martin
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 2.  Characterization of Severity in Zellweger Spectrum Disorder by Clinical Findings: A Scoping Review, Meta-Analysis and Medical Chart Review.

Authors:  Mousumi Bose; Christine Yergeau; Yasmin D'Souza; David D Cuthbertson; Melisa J Lopez; Alyssa K Smolen; Nancy E Braverman
Journal:  Cells       Date:  2022-06-10       Impact factor: 7.666

3.  Contribution of fetal MR imaging in the prenatal diagnosis of Zellweger syndrome.

Authors:  F Mochel; A-G Grébille; A Benachi; J Martinovic; F Razavi; D Rabier; I Simon; N Boddaert; F Brunelle; P Sonigo
Journal:  AJNR Am J Neuroradiol       Date:  2006-02       Impact factor: 3.825

  3 in total

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