Literature DB >> 22833188

Mosaic DCX deletion causes subcortical band heterotopia in males.

Chloé Quélin1, Yoann Saillour, Isabelle Souville, Karine Poirier, Marie Ange N'guyen-Morel, Laurent Vercueil, Anne Elodie Millisher-Bellaiche, Nathalie Boddaert, Fanny Dubois, Jamel Chelly, Cherif Beldjord, Nadia Bahi-Buisson.   

Abstract

Subcortical band heterotopia (SBH) is a neuronal migration disorder usually described in females carrying heterozygous mutations in the X-linked doublecortin (DCX) gene. Hemizygous DCX mutations in males result in lissencephaly. Recently, exonic deletions of DCX resulting in a severer form of agyria have been reported. Nevertheless, rare male patients with SBH have been described with somatic mosaicism of point mutations. Here, we identified a somatic mosaicism for a deletion of exon 4 in the DCX gene in a male patient with SBH detected prenatally. This finding points to the possible implication of mosaic deletions in the DCX gene in unexplained forms of SBH and may allow for detection of SBH prenatally.

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Year:  2012        PMID: 22833188     DOI: 10.1007/s10048-012-0339-4

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  23 in total

Review 1.  Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).

Authors:  Carlos Cardoso; Richard J Leventer; James J Dowling; Heather L Ward; June Chung; Kristin S Petras; Jessica A Roseberry; Ann M Weiss; Soma Das; Christa Lese Martin; Daniela T Pilz; William B Dobyns; David H Ledbetter
Journal:  Hum Mutat       Date:  2002-01       Impact factor: 4.878

2.  A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.

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Journal:  Cell       Date:  1998-01-09       Impact factor: 41.582

3.  Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly.

Authors:  W B Dobyns; C L Truwit; M E Ross; N Matsumoto; D T Pilz; D H Ledbetter; J G Gleeson; C A Walsh; A J Barkovich
Journal:  Neurology       Date:  1999-07-22       Impact factor: 9.910

Review 4.  X-linked malformations of neuronal migration.

Authors:  W B Dobyns; E Andermann; F Andermann; D Czapansky-Beilman; F Dubeau; O Dulac; R Guerrini; B Hirsch; D H Ledbetter; N S Lee; J Motte; J M Pinard; R A Radtke; M E Ross; D Tampieri; C A Walsh; C L Truwit
Journal:  Neurology       Date:  1996-08       Impact factor: 9.910

5.  Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

Authors:  N Matsumoto; R J Leventer; J A Kuc; S K Mewborn; L L Dudlicek; M B Ramocki; D T Pilz; P L Mills; S Das; M E Ross; D H Ledbetter; W B Dobyns
Journal:  Eur J Hum Genet       Date:  2001-01       Impact factor: 4.246

6.  Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis.

Authors:  S C Yau; M Bobrow; C G Mathew; S J Abbs
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

7.  Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia.

Authors:  D Mei; E Parrini; M Pasqualetti; G Tortorella; E Franzoni; U Giussani; C Marini; S Migliarini; R Guerrini
Journal:  Neurology       Date:  2007-02-06       Impact factor: 9.910

8.  LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Authors:  D T Pilz; N Matsumoto; S Minnerath; P Mills; J G Gleeson; K M Allen; C A Walsh; A J Barkovich; W B Dobyns; D H Ledbetter; M E Ross
Journal:  Hum Mol Genet       Date:  1998-12       Impact factor: 6.150

9.  Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.

Authors:  Detlef Boehm; Sabine Herold; Alma Kuechler; Thomas Liehr; Franco Laccone
Journal:  Hum Mutat       Date:  2004-04       Impact factor: 4.878

10.  Band heterotopia: correlation of outcome with magnetic resonance imaging parameters.

Authors:  A J Barkovich; R Guerrini; G Battaglia; G Kalifa; T N'Guyen; A Parmeggiani; M Santucci; P Giovanardi-Rossi; T Granata; L D'Incerti
Journal:  Ann Neurol       Date:  1994-10       Impact factor: 10.422

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  3 in total

1.  Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders.

Authors:  Dolores González-Morón; Sebastián Vishnopolska; Damián Consalvo; Nancy Medina; Marcelo Marti; Marta Córdoba; Cecilia Vazquez-Dusefante; Santiago Claverie; Sergio Alejandro Rodríguez-Quiroga; Patricia Vega; Walter Silva; Silvia Kochen; Marcelo Andrés Kauffman
Journal:  PLoS One       Date:  2017-09-27       Impact factor: 3.240

2.  Double Cortex Syndrome (Subcortical Band Heterotopia): A Case Report.

Authors:  Ali Akbar Momen; Mehdi Momen
Journal:  Iran J Child Neurol       Date:  2015

Review 3.  Toward a Better Understanding of Neuronal Migration Deficits in Autism Spectrum Disorders.

Authors:  Yi-Hsuan Pan; Nan Wu; Xiao-Bing Yuan
Journal:  Front Cell Dev Biol       Date:  2019-09-20
  3 in total

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