Literature DB >> 8306355

Fetal type II lissencephaly: a case report.

M V Squier1.   

Abstract

Type II lissencephaly is a rare cortical malformation associated with a number of clinical syndromes, including Walker-Warburg syndrome and some forms of congenital muscular dystrophy. The neuropathology of a 20-week fetus is described showing the pathogenesis of the malformation, which appears to result from abnormal migration of neurons through the pial-glial barrier into the leptomeninges.

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Year:  1993        PMID: 8306355     DOI: 10.1007/BF00306192

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  7 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.  Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis.

Authors:  R S Williams; C N Swisher; M Jennings; M Ambler; V S Caviness
Journal:  Neurology       Date:  1984-12       Impact factor: 9.910

3.  Oculocerebral malformations. A reappraisal of Walker's 'lissencephaly'.

Authors:  C C Chan; P R Egbert; M K Herrick; H Urich
Journal:  Arch Neurol       Date:  1980-02

4.  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

5.  Cerebro-ocular dysplasia--muscular dystrophy (Walker Warburg) syndrome. Findings in 20-week-old fetus.

Authors:  G Miller; R L Ladda; J Towfighi
Journal:  Acta Neuropathol       Date:  1991       Impact factor: 17.088

6.  Cerebro-ocular dysplasia-muscular dystrophy (COD-MD) syndrome.

Authors:  J Towfighi; J W Sassani; K Suzuki; R L Ladda
Journal:  Acta Neuropathol       Date:  1984       Impact factor: 17.088

7.  Diagnostic criteria for Walker-Warburg syndrome.

Authors:  W B Dobyns; R A Pagon; D Armstrong; C J Curry; F Greenberg; A Grix; L B Holmes; R Laxova; V V Michels; M Robinow
Journal:  Am J Med Genet       Date:  1989-02
  7 in total

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