Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/197734
Type: Artigo de periódico
Title: A New Candidate Locus For Bilateral Perisylvian Polymicrogyria Mapped On Chromosome Xq27.
Author: Santos, Neide F
Secolin, Rodrigo
Brandão-Almeida, Iara L
Silva, Marilza S
Torres, Fábio R
Tsuneda, Simone S
Guimarães, Catarina A
Hage, Simone R V
Cendes, Fernando
Guerreiro, Marilisa M
Lopes-Cendes, Iscia
Abstract: Polymicrogyria (PMG) is characterized by an excessive number of small and prominent brain gyri, separated by shallow sulci. Bilateral perisylvian polymicrogyria (BPP) is the most common form of PMG. Clinical signs include pseudobulbar paresis, mental retardation, and epilepsy. Familial forms of BPP have been described and a candidate locus was previously mapped to chromosome Xq28, distal do marker DXS8103. The objective of this study was to perform linkage analysis in one family segregating BPP. A total of 15 individuals, including 8 affected patients with BPP were evaluated. Family members were examined by a neurologist and subjected to magnetic resonance imaging scans. Individuals were genotyped for 18 microsatellite markers, flanking a 42.3 cM interval on ch Xq27-q28. Two-point and multipoint linkage analysis was performed using the LINKAGE package and haplotype reconstruction was performed by GENEHUNTER software. Our results showed a wide spectrum of clinical manifestations in affected individuals with BPP, ranging from normal to mild neurological abnormalities. Two-point linkage analysis yield a Zmax = 2.06 at theta = 0.00 for markers DXS1205 and DXS1227. Multipoint lod-scores indicate a candidate interval of 13 cM between markers DSXS1205 and DXS8043, on ch Xq27.2-Xq27.3. These results point to a new locus for BPP in a more centromeric location than previously reported.
Subject: Adult
Cerebral Cortex
Child
Chromosome Mapping
Chromosomes, Human, X
Female
Genotype
Haplotypes
Humans
Lod Score
Magnetic Resonance Imaging
Male
Malformations Of Cortical Development
Microsatellite Repeats
Pedigree
Citation: American Journal Of Medical Genetics. Part A. v. 146A, n. 9, p. 1151-7, 2008-May.
Rights: fechado
Identifier DOI: 10.1002/ajmg.a.32270
Address: http://www.ncbi.nlm.nih.gov/pubmed/18384144
Date Issue: 2008
Appears in Collections:Unicamp - Artigos e Outros Documentos

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