Case studyBilateral symmetrical frontoparietal polymicrogyria
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Cited by (10)
Three Patients With Severe Bilateral Frontoparietal Polymicrogyria
2008, Pediatric NeurologyCitation Excerpt :Given, however, that polymicrogyria itself is associated with many known genetic disorders, including chromosomal 22q11 deletion syndromes [11], mtDNA point mutation [12], and Ehlers-Danlos syndrome [13], other factors must be involved in the pathogenesis. In the present three cases, the anatomic structure of the brain showed more severe diffuse cortical and subcortical involvements than those seen in the bilateral frontoparietal polymicrogyria cases previously reported by Piao et al. [1,2] and others [6-8]. All three sporadic in origin, and there were no convulsive disorders in their families.
Bilateral fronto-parietal polymicrogyria in an Indian infant
2011, Journal of Pediatric NeurologyManagement of the child with polymicrogyria
2009, Journal of Neuroscience NursingMalformations of cortical development and epilepsy: Evaluation of 101 cases (Part II)
2007, Turkish Journal of PediatricsGenotype-phenotype analysis of human frontoparietal polymicrogyria syndromes
2005, Annals of Neurology
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Correspondence: L Sztriha, Department of Paediatrics, FMHS, UAE University, Al Ain, PO Box: 17666, United Arab Emirates; Phone: +971 3 703 9414; Fax: +971 3 767 2022e-mail:[email protected]