Literature DB >> 19576302

4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate.

Jill Urquhart1, Graeme C M Black, Jill Clayton-Smith.   

Abstract

We report a 4.5 Mb deletion of 2q33.1 in an individual with developmental delay and cleft palate. There have been various previous reports of deletions of 2q3, all with varying breakpoints and all larger than the current case. Whilst there is some variation in the phenotypes of patients with 2q3 deletions all share a commonly deleted region within 2q33.1 which includes SATB2, a gene previously shown to be associated with cleft palate. The phenotypic features of our patient are milder than those reported so far.

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Year:  2009        PMID: 19576302     DOI: 10.1016/j.ejmg.2009.06.003

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  15 in total

1.  SATB2 in neuroendocrine neoplasms: strong expression is restricted to well-differentiated tumours of lower gastrointestinal tract origin and is most frequent in Merkel cell carcinoma among poorly differentiated carcinomas.

Authors:  Andrew M Bellizzi
Journal:  Histopathology       Date:  2019-11-15       Impact factor: 5.087

2.  Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.

Authors:  Milena Simioni; François Artiguenave; Vincent Meyer; Ilária C Sgardioli; Nilma L Viguetti-Campos; Isabella Lopes Monlleó; Andréa T Maciel-Guerra; Carlos E Steiner; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-06-01

3.  Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.

Authors:  Annabel Whibley; Jill Urquhart; Jonathan Dore; Lionel Willatt; Georgina Parkin; Lorraine Gaunt; Graeme Black; Dian Donnai; F Lucy Raymond
Journal:  Eur J Hum Genet       Date:  2010-05-19       Impact factor: 4.246

4.  A cross-species analysis of Satb2 expression suggests deep conservation across vertebrate lineages.

Authors:  Kelly Sheehan-Rooney; Božena Pálinkášová; Johann K Eberhart; Michael J Dixon
Journal:  Dev Dyn       Date:  2010-12       Impact factor: 3.780

5.  Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.

Authors:  Petcharat Leoyklang; Kanya Suphapeetiporn; Chalurmpon Srichomthong; Siraprapa Tongkobpetch; Stefanie Fietze; Heidi Dorward; Andrew R Cullinane; William A Gahl; Marjan Huizing; Vorasuk Shotelersuk
Journal:  Hum Genet       Date:  2013-08-08       Impact factor: 4.132

6.  SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population.

Authors:  Venkatesh Babu Gurramkonda; Altaf Hussain Syed; Jyotsna Murthy; Bhaskar V K S Lakkakula
Journal:  J Oral Biol Craniofac Res       Date:  2015-07-29

7.  Further delineation of the SATB2 phenotype.

Authors:  Dennis Döcker; Max Schubach; Moritz Menzel; Marita Munz; Christiane Spaich; Saskia Biskup; Deborah Bartholdi
Journal:  Eur J Hum Genet       Date:  2013-12-04       Impact factor: 4.246

8.  First Korean case of SATB2-associated 2q32-q33 microdeletion syndrome.

Authors:  Nae Yu; Saeam Shin; Kyung-A Lee
Journal:  Ann Lab Med       Date:  2015-02-12       Impact factor: 3.464

9.  Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromes.

Authors:  Adrian Mc Cormack; Juliet Taylor; Nerine Gregersen; Alice M George; Donald R Love
Journal:  Case Rep Genet       Date:  2013-06-09

10.  Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.

Authors:  Jacqueline K Rainger; Shipra Bhatia; Hemant Bengani; Philippe Gautier; Joe Rainger; Matt Pearson; Morad Ansari; Jayne Crow; Felicity Mehendale; Bozena Palinkasova; Michael J Dixon; Pamela J Thompson; Mar Matarin; Sanjay M Sisodiya; Dirk A Kleinjan; David R Fitzpatrick
Journal:  Hum Mol Genet       Date:  2013-12-20       Impact factor: 6.150

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