Literature DB >> 2703857

Structural and chemical alterations in the cerebral maldevelopment of fetal cerebro-hepato-renal (Zellweger) syndrome.

J M Powers1, R C Tummons, V S Caviness, A B Moser, H W Moser.   

Abstract

The cerebra of four abortuses (estimated gestational age 14-22 weeks), diagnosed as cerebro-hepato-renal (Zellweger) syndrome in utero, were examined morphologically with light microscopic, immunocytochemical and ultrastructural techniques and biochemically with gas liquid chromatographic assays for cholesterol ester fatty acids and plasmalogens. Centrosylvian architectonic abnormalities consisting, in part, of thin cortical plates and broad subcortical heterotopic zones were found in all abortuses. Astrocytes, neuroblasts, immature neurons and radial glia contained abnormal pleomorphic cytosomes, presumably of variable lipid composition. The same areas exhibited increases in cholesterol ester very long chain fatty acids and decreased plasmalogens. A pathogenetic hypothesis, proposing that regional tissue constraints act in concert with a peroxisomal-derived biochemical abnormality to impede centrosylvian neuronal migration, is discussed.

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Year:  1989        PMID: 2703857     DOI: 10.1097/00005072-198905000-00005

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  8 in total

Review 1.  The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction.

Authors:  P L Faust; H M Su; A Moser; H W Moser
Journal:  J Mol Neurosci       Date:  2001 Apr-Jun       Impact factor: 3.444

Review 2.  Normal and defective neuronal membranes: structure and function: neuronal lesions in peroxisomal disorders.

Authors:  J M Powers
Journal:  J Mol Neurosci       Date:  2001 Apr-Jun       Impact factor: 3.444

3.  Cerebral abnormalities in thanatophoric dysplasia.

Authors:  C L Coulter; R W Leech; R A Brumback; G B Schaefer
Journal:  Childs Nerv Syst       Date:  1991-02       Impact factor: 1.475

4.  Subependymal germinolytic cysts in Zellweger syndrome.

Authors:  I M Russel; L van Sonderen; H L van Straaten; P G Barth
Journal:  Pediatr Radiol       Date:  1995

Review 5.  Neuropathology of peroxisomal diseases.

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

6.  Prenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouse.

Authors:  S Huyghe; M Casteels; A Janssen; L Meulders; G P Mannaerts; P E Declercq; P P Van Veldhoven; M Baes
Journal:  Biochem J       Date:  2001-02-01       Impact factor: 3.857

7.  Alterations of fatty acid metabolism and membrane fluidity in peroxisome-defective mutant ZP102 cells.

Authors:  Michiaki Nagura; Makiko Saito; Masao Iwamori; Yoichi Sakakihara; Takashi Igarashi
Journal:  Lipids       Date:  2004-01       Impact factor: 1.880

8.  Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.

Authors:  P L Faust; M E Hatten
Journal:  J Cell Biol       Date:  1997-12-01       Impact factor: 10.539

  8 in total

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