Literature DB >> 7507292

Developmental data on individuals with the Brachmann-de Lange syndrome.

A D Kline1, C Stanley, J Belevich, K Brodsky, M Barr, L G Jackson.   

Abstract

One hundred twenty-two patients with clinically confirmed Brachmann-de Lange syndrome (BDLS) were evaluated developmentally. Recruitment was made from our genetics department and through meetings of the Cornelia de Lange Syndrome Foundation parent support group. Developmental information was obtained from records of physicians, schools and developmental centers, or from parents on each of the 122 individuals, allowing division into four groups for study: group 1 (n = 48) underwent formal developmental assessments, which generated intelligence or developmental quotients, and had a completed parental questionnaire with specific developmental questions regarding ages of skills mastered; group II (n = 23) had additional developmental records available without formal testing, as well as the questionnaire; group III (n = 22) had only a completed questionnaire; and group IV (n = 29) had formal developmental testing or other developmental records but no available questionnaire. These data were analyzed in order to be able to predict attainable psychomotor development. Average scores on formal testing were found to be in the mild to moderate level of mental retardation, ranging from below 30 to 85, with an average intelligence quotient of 53, higher than previously reported. Visual-spatial memory and perceptual organization skills were found to be strengths. Younger individuals born before 1980 demonstrated higher scores on testing. Early intervention appears to play a major role in the level of developmental achievement.

Entities:  

Mesh:

Year:  1993        PMID: 7507292     DOI: 10.1002/ajmg.1320470724

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


  11 in total

1.  Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction.

Authors:  Diana Braunholz; Melanie Hullings; María Concepcion Gil-Rodríguez; Christopher T Fincher; Mark B Mallozzi; Elizabeth Loy; Melanie Albrecht; Maninder Kaur; Janusz Limon; Abhinav Rampuria; Dinah Clark; Antonie Kline; Andreas Dalski; Juliane Eckhold; Andreas Tzschach; Raoul Hennekam; Gabriele Gillessen-Kaesbach; Jolanta Wierzba; Ian D Krantz; Matthew A Deardorff; Frank J Kaiser
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

Review 2.  CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.

Authors:  Benjamin J Landis; David S Cooper; Robert B Hinton
Journal:  Cardiol Young       Date:  2015-09-08       Impact factor: 1.093

3.  Mutational Screening and Prenatal Diagnosis in Cornelia de Lange syndrome.

Authors:  Usha Dave; Dhanlaxmi Shetty
Journal:  J Obstet Gynaecol India       Date:  2013-09-29

4.  Investigation of autistic features among individuals with mild to moderate Cornelia de Lange syndrome.

Authors:  Mariko Nakanishi; Matthew A Deardorff; Dinah Clark; Susan E Levy; Ian Krantz; Mary Pipan
Journal:  Am J Med Genet A       Date:  2012-06-27       Impact factor: 2.802

5.  NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations.

Authors:  Lynette A Gillis; Jennifer McCallum; Maninder Kaur; Cheryl DeScipio; Dinah Yaeger; Allison Mariani; Antonie D Kline; Hui-hua Li; Marcella Devoto; Laird G Jackson; Ian D Krantz
Journal:  Am J Hum Genet       Date:  2004-08-18       Impact factor: 11.025

Review 6.  Cohesin and human disease.

Authors:  Jinglan Liu; Ian D Krantz
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

Review 7.  Natural history of aging in Cornelia de Lange syndrome.

Authors:  Antonie D Kline; Marco Grados; Paul Sponseller; Howard P Levy; Natalie Blagowidow; Christianne Schoedel; Joni Rampolla; Douglas K Clemens; Ian Krantz; Amy Kimball; Carmen Pichard; David Tuchman
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-08-15       Impact factor: 3.908

Review 8.  Cornelia de Lange syndrome, cohesin, and beyond.

Authors:  J Liu; I D Krantz
Journal:  Clin Genet       Date:  2009-10       Impact factor: 4.438

9.  Copy number analysis of NIPBL in a cohort of 510 patients reveals rare copy number variants and a mosaic deletion.

Authors:  Yu-Wei Cheng; Christopher A Tan; Agata Minor; Kelly Arndt; Latrice Wysinger; Dorothy K Grange; Beth A Kozel; Nathaniel H Robin; Darrel Waggoner; Carrie Fitzpatrick; Soma Das; Daniela Del Gaudio
Journal:  Mol Genet Genomic Med       Date:  2013-11-14       Impact factor: 2.183

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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