Literature DB >> 17431901

Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33).

Martin Poot1, Hester Y Kroes, Suzanne E V D Wijst, Marc J Eleveld, Liesbeth Rooms, Rutger A J Nievelstein, Daniel Olde Weghuis, Rene C Vreuls, Gerard Hageman, Frank Kooy, Ron Hochstenbach.   

Abstract

A 10-year-old boy with vermis hypoplasia, dilatation of the fourth ventricle, enlarged cisterna magna and aplasia of the corpus callosum, consistent with the Dandy-Walker complex (DWC), and slight facial dysmorphisms, severe motor and mental retardation is presented. By combining data obtained by karyotyping, array-CGH, FISH, and multiplex ligation-mediated probe amplification (MLPA) we identified a 5 Mb deletion of the 1q44 --> qter region resulting from a paternal t(1;20)(q44;q13.33). This smallest 1q44 deletion reported so far, enabled us to significantly narrow down the number of candidate genes for the DWC in this region. Since the ZNF124 transcription factor is strongly expressed in the fetal brain it may represent a candidate gene for the DWC at 1q44.

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Year:  2007        PMID: 17431901     DOI: 10.1002/ajmg.a.31690

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  12 in total

1.  Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43-q44.

Authors:  Sandesh C Sreenath Nagamani; Ayelet Erez; Carolyn Bay; Anjana Pettigrew; Seema R Lalani; Kristin Herman; Brett H Graham; Malgorzata Jm Nowaczyk; Monica Proud; William J Craigen; Bobbi Hopkins; Beth Kozel; Katie Plunkett; Patricia Hixson; Pawel Stankiewicz; Ankita Patel; Sau Wai Cheung
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

2.  Pre- and Postnatal Analysis of Chromosome 1q44 Deletion in Agenesis of Corpus Callosum.

Authors:  Mitesh Shetty; Ambika Srikanth; Jayarama Kadandale; Sridevi Hegde
Journal:  Mol Syndromol       Date:  2015-09-11

Review 3.  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2014-01-28       Impact factor: 13.501

4.  High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.

Authors:  Blake C Ballif; Jill A Rosenfeld; Ryan Traylor; Aaron Theisen; Patricia I Bader; Roger L Ladda; Susan L Sell; Michelle Steinraths; Urvashi Surti; Marianne McGuire; Shelley Williams; Sandra A Farrell; James Filiano; Rhonda E Schnur; Lauren B Coffey; Raymond C Tervo; Tracy Stroud; Michael Marble; Michael Netzloff; Kristen Hanson; Arthur S Aylsworth; J S Bamforth; Deepti Babu; Dmitriy M Niyazov; J Britt Ravnan; Roger A Schultz; Allen N Lamb; Beth S Torchia; Bassem A Bejjani; Lisa G Shaffer
Journal:  Hum Genet       Date:  2011-07-29       Impact factor: 4.132

5.  Differences in human and chimpanzee gene expression patterns define an evolving network of transcription factors in brain.

Authors:  Katja Nowick; Tim Gernat; Eivind Almaas; Lisa Stubbs
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-10       Impact factor: 11.205

Review 6.  A developmental and genetic classification for midbrain-hindbrain malformations.

Authors:  A James Barkovich; Kathleen J Millen; William B Dobyns
Journal:  Brain       Date:  2009-12       Impact factor: 13.501

7.  Recurrent copy number changes in mentally retarded children harbour genes involved in cellular localization and the glutamate receptor complex.

Authors:  Martin Poot; Marc J Eleveld; Ruben van 't Slot; Hans Kristian Ploos van Amstel; Ron Hochstenbach
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

8.  Gain of FAM123B and ARHGEF9 in an Obese Man with Intellectual Disability, Congenital Heart Defects and Multiple Supernumerary Ring Chromosomes.

Authors:  R Hochstenbach; M E van Gijn; P-J Krijtenburg; R Raemakers; R van 't Slot; I Renkens; M J Eleveld; J J van der Smagt; M Poot
Journal:  Mol Syndromol       Date:  2012-11-20

9.  Identifying human disease genes through cross-species gene mapping of evolutionary conserved processes.

Authors:  Martin Poot; Alexandra Badea; Robert W Williams; Martien J Kas
Journal:  PLoS One       Date:  2011-05-04       Impact factor: 3.240

10.  Maternal 5mCpG Imprints at the PARD6G-AS1 and GCSAML Differentially Methylated Regions Are Decoupled From Parent-of-Origin Expression Effects in Multiple Human Tissues.

Authors:  Graziela de Sá Machado Araújo; Ronaldo da Silva Francisco Junior; Cristina Dos Santos Ferreira; Pedro Thyago Mozer Rodrigues; Douglas Terra Machado; Thais Louvain de Souza; Jozimara Teixeira de Souza; Cleiton Figueiredo Osorio da Silva; Antônio Francisco Alves da Silva; Claudia Caixeta Franco Andrade; Alan Tardin da Silva; Victor Ramos; Ana Beatriz Garcia; Filipe Brum Machado; Enrique Medina-Acosta
Journal:  Front Genet       Date:  2018-03-01       Impact factor: 4.599

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