Literature DB >> 10734259

Bilateral frontoparietal polymicrogyria and epilepsy.

L Sztriha1, M Nork.   

Abstract

Two patients with bilateral frontoparietal polymicrogyria are reported. Severe developmental delay, mental retardation, spastic tetraplegia, and seizures were the main clinical features. Magnetic resonance imaging revealed a bilateral thick cortex with irregular gyri and a festoonlike gray-white matter junction. Bilateral frontoparietal polymicrogyria may represent a further form of the bilateral polymicrogyria syndromes in addition to perisylvian and parasagittal parieto-occipital polymicrogyria.

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Year:  2000        PMID： 10734259     DOI： 10.1016/s0887-8994(99)00142-3

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN： 0887-8994            Impact factor:   3.372


  4 in total

1.  An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21.

Authors:  Xianhua Piao; Lina Basel-Vanagaite; Rachel Straussberg; P Ellen Grant; Elizabeth W Pugh; Kim Doheny; Betty Doan; Susan E Hong; Yin Yao Shugart; Christopher A Walsh
Journal:  Am J Hum Genet       Date:  2002-02-13       Impact factor: 11.025

2.  Polymicrogyria: correlation of magnetic resonance imaging and clinical findings.

Authors:  Ertugrul Mavili; Abdulhakim Coskun; Huseyin Per; Halil Donmez; Sefer Kumandas; Ali Yikilmaz
Journal:  Childs Nerv Syst       Date:  2012-06       Impact factor: 1.475

Review 3.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

4.  GPR56-regulated granule cell adhesion is essential for rostral cerebellar development.

Authors:  Samir Koirala; Zhaohui Jin; Xianhua Piao; Gabriel Corfas
Journal:  J Neurosci       Date:  2009-06-10       Impact factor: 6.167
  4 in total

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