Literature DB >> 8291539

Brachmann-de Lange syndrome. Delineation of the clinical phenotype.

M Ireland1, D Donnai, J Burn.   

Abstract

A total of 31 cases previously diagnosed as having Brachmann-de Lange syndrome were ascertained and examined, of which 11 were thought to have been misdiagnosed. Of those correctly diagnosed, there appeared to be a phenotypic dichotomy with classical and mild cases. Those facial findings of greatest diagnostic value were the combination of the characteristic eyebrows, long philtrum, thin lips and crescent-shaped mouth. The characteristic eyebrows were neat, well defined and arched as though they had been pencilled. This combination of anomalies was absent in postpubertal males but not in postpubertal females. Facial abnormalities most likely to lead to incorrect use of the eponym were hypertrichosis, synophrys, and bushy eyebrows.

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Year:  1993        PMID: 8291539     DOI: 10.1002/ajmg.1320470705

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  34 in total

1.  Behavioural phenotype of Cornelia de Lange syndrome.

Authors:  T P Berney; M Ireland; J Burn
Journal:  Arch Dis Child       Date:  1999-10       Impact factor: 3.791

2.  De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes.

Authors:  J E Allanson; R C Hennekam; M Ireland
Journal:  J Med Genet       Date:  1997-08       Impact factor: 6.318

3.  Classical cornelia de lange syndrome.

Authors:  Ev Badoe
Journal:  Ghana Med J       Date:  2006

4.  Genomic duplication resulting in increased copy number of genes encoding the sister chromatid cohesion complex conveys clinical consequences distinct from Cornelia de Lange.

Authors:  J Yan; F Zhang; E Brundage; A Scheuerle; B Lanpher; R P Erickson; Z Powis; H B Robinson; P L Trapane; D Stachiw-Hietpas; K M Keppler-Noreuil; S R Lalani; T Sahoo; A C Chinault; A Patel; S W Cheung; J R Lupski
Journal:  J Med Genet       Date:  2008-12-03       Impact factor: 6.318

5.  Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.

Authors:  Matthew A Deardorff; Maninder Kaur; Dinah Yaeger; Abhinav Rampuria; Sergey Korolev; Juan Pie; Concepcion Gil-Rodríguez; María Arnedo; Bart Loeys; Antonie D Kline; Meredith Wilson; Kaj Lillquist; Victoria Siu; Feliciano J Ramos; Antonio Musio; Laird S Jackson; Dale Dorsett; Ian D Krantz
Journal:  Am J Hum Genet       Date:  2007-01-17       Impact factor: 11.025

Review 6.  Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes.

Authors:  Dale Dorsett
Journal:  Chromosoma       Date:  2006-07-04       Impact factor: 4.316

7.  Effects of sister chromatid cohesion proteins on cut gene expression during wing development in Drosophila.

Authors:  Dale Dorsett; Joel C Eissenberg; Ziva Misulovin; Andrew Martens; Bethany Redding; Kim McKim
Journal:  Development       Date:  2005-10-05       Impact factor: 6.868

8.  Cornelia de lange syndrome.

Authors:  Naeimeh Tayebi
Journal:  Indian J Hum Genet       Date:  2008-01

9.  Cornelia de Lange Syndrome with NIPBL gene mutation: a case report.

Authors:  Kyung-Hee Park; Seung-Tae Lee; Chang-Seok Ki; Shin-Yun Byun
Journal:  J Korean Med Sci       Date:  2010-11-24       Impact factor: 2.153

10.  Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome.

Authors:  Shimako Kawauchi; Anne L Calof; Rosaysela Santos; Martha E Lopez-Burks; Clint M Young; Michelle P Hoang; Abigail Chua; Taotao Lao; Mark S Lechner; Jeremy A Daniel; Andre Nussenzweig; Leonard Kitzes; Kyoko Yokomori; Benedikt Hallgrimsson; Arthur D Lander
Journal:  PLoS Genet       Date:  2009-09-18       Impact factor: 5.917

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