Literature DB >> 6737009

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

K Takada, H Nakamura, J Tanaka.   

Abstract

We report five cases of congenital muscular dystrophy with central nervous system involvement of the Fukuyama type (FCMD) in which cerebral cortical dysplasia was not uniform even in the same brain. We have categorized the dysplasia into three major patterns, each with a predictable topography despite individual variations. Cerebellar micropolygyria was localized to the dorsal halves of each hemisphere. Aberrant fascicles of myelinated nerve fibers, closely associated with micropolygyria, were found in the subarachnoid space of the dorsal cerebellar surface in all but one case. We discuss the characteristics of the cortical dysplasia of FCMD, particularly in relation to that of Walker's lissencephaly, pathogenesis, and the relationship between lesions of the central nervous system and skeletal muscle.

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Year:  1984        PMID: 6737009     DOI: 10.1097/00005072-198407000-00005

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


  15 in total

1.  Cortical dysplasia associated with massive ectopia of neurons and glial cells within the subarachnoid space.

Authors:  B H Choi; S C Matthias
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

2.  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

3.  Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD).

Authors:  K Takada; H Nakamura; K Suzumori; T Ishikawa; N Sugiyama
Journal:  Acta Neuropathol       Date:  1987       Impact factor: 17.088

4.  Long survival in Fukuyama congenital muscular dystrophy: occurrence of neurofibrillary tangles in the nucleus basalis of Meynert and locus ceruleus.

Authors:  K Takada; Y S Rin; S Kasagi; K Sato; H Nakamura; J Tanaka
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

5.  MRI of the brain in muscle-eye-brain (MEB) disease.

Authors:  L Valanne; H Pihko; K Katevuo; P Karttunen; H Somer; P Santavuori
Journal:  Neuroradiology       Date:  1994-08       Impact factor: 2.804

6.  Shaking rat Kawasaki (SRK): a new neurological mutant rat in the Wistar strain.

Authors:  H Aikawa; I Nonaka; M Woo; T Tsugane; K Esaki
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

7.  Serial MRI in Fukuyama type congenital muscular dystrophy.

Authors:  M Aihara; Y Tanabe; K Kato
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

8.  The changing MR imaging appearance of polymicrogyria: a consequence of myelination.

Authors:  Jun-ichi Takanashi; A James Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2003-05       Impact factor: 3.825

9.  Lissencephaly with congenital muscular dystrophy and ocular abnormalities: cerebro-oculo-muscular syndrome.

Authors:  M Sasaki; K Yoshioka; T Yanagisawa; A Nemoto; Y Takasago; T Nagano
Journal:  Childs Nerv Syst       Date:  1989-02       Impact factor: 1.475

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

Authors:  K Takada; H Nakamura; S Takashima
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

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