Literature DB >> 2457291

Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis.

K Takada1, H Nakamura, S Takashima.   

Abstract

The Golgi and vascular impregnation methods were applied to the abnormal cerebral cortex in Fukuyama congenital muscular dystrophy (FCMD). The cortical dysplasia in FCMD has been categorized into three patterns by the degrees of cytoarchitectural abnormalities. Cortical dysplasia type 1 is characterized by the presence of verrucose nodules in the otherwise normally stratified cortex. By the Golgi method, many neurons at the top of the verrucose nodules showed abnormal morphology and dendritic orientation, while the rest of pyramidal neurons appeared relatively normal. A single 'central blood vessel' often penetrated vertically at the axis of the verrucose nodules, so that it was suggested that such nodules were formed around the long perforating blood vessels. In type 2 dysplasia, or unlayered micropolygyria, individual cells showed relative paucity of lateral dendritic arborization. Despite mutual parallel alignment, neurons were often tilted in varying degrees. Concentration of relatively large blood vessels was seen at the microsulci. In the severest dysplastic pattern, or type 3 dysplasia, in addition to highly distorted cellular alignment, dendritic arborization of individual neurons were very poor. The cortical vasculature in type 3 consisted of two heterogeneous patterns; an extreme vascular distortion in the upper layer and a relatively well-preserved radial pattern in the deep layer. The upper layer is supposed to represent the extra-cortical gliomesenchymal layer intermixed with neuronal clusters seen in the 23-week FCMD fetus we reported previously. By that fetal case analysis, we had hypothesized that cortical dysplasia in FCMD has resulted from superficial heterotopia of migrating neurons related to diffuse proliferation of the extra-cortical gliomesenchymal tissue and focal or extensive defects of glia limitans. The abnormalities in cellular morphology, cellular alignment, and cortical vascular patterns shown in the present study seem to be compatible with our hypothesis.

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Year:  1988        PMID: 2457291     DOI: 10.1007/bf00688101

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  22 in total

1.  Verrucose dysplasia of the cerebral cortex. (Dysgenesie nodulaire disseminee of Morel and Wildi).

Authors:  N GRCEVIC; F ROBERT
Journal:  J Neuropathol Exp Neurol       Date:  1961-07       Impact factor: 3.685

2.  The status verrucosus of the cerebral cortex.

Authors:  I BERTRAND; J GRUNER
Journal:  J Neuropathol Exp Neurol       Date:  1955-10       Impact factor: 3.685

3.  Pachygyria: relation of findings to modern embryologic concepts.

Authors:  J Hanaway; S I Lee; N G Netsky
Journal:  Neurology       Date:  1968-08       Impact factor: 9.910

4.  Embryonic vertebrate central nervous system: revised terminology. The Boulder Committee.

Authors: 
Journal:  Anat Rec       Date:  1970-02

5.  The cellular pathology of microgyria. A Golgi analysis.

Authors:  R S Williams; R J Ferrante; V S Caviness
Journal:  Acta Neuropathol       Date:  1976-11-15       Impact factor: 17.088

6.  Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type).

Authors:  K Takada; H Nakamura; J Tanaka
Journal:  J Neuropathol Exp Neurol       Date:  1984-07       Impact factor: 3.685

Review 7.  Neuronal migration, with special reference to developing human brain: a review.

Authors:  R L Sidman; P Rakic
Journal:  Brain Res       Date:  1973-11-09       Impact factor: 3.252

8.  The growth and development of microvasculature in human cerebral cortex.

Authors:  M G Norman; J R O'Kusky
Journal:  J Neuropathol Exp Neurol       Date:  1986-05       Impact factor: 3.685

9.  A Golgi analysis of unlayered polymicrogyria.

Authors:  I Ferrer
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

10.  Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.

Authors:  W B Dobyns; R F Stratton; F Greenberg
Journal:  Am J Med Genet       Date:  1984-07
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  4 in total

1.  MRI analysis of sulcation morphology in polymicrogyria.

Authors:  Anthony James Barkovich
Journal:  Epilepsia       Date:  2010-02       Impact factor: 5.864

2.  Unlayered polymicrogyria: structural and developmental aspects.

Authors:  I Ferrer; I Catalá
Journal:  Anat Embryol (Berl)       Date:  1991

3.  Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brains.

Authors:  A Gelot; T Billette de Villemeur; C Bordarier; M M Ruchoux; C Moraine; G Ponsot
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

4.  Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations.

Authors:  Elena Parrini; Anna Rita Ferrari; Thomas Dorn; Christopher A Walsh; Renzo Guerrini
Journal:  Epilepsia       Date:  2008-10-06       Impact factor: 5.864

  4 in total

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