Literature DB >> 8291540

Variability of the Brachmann-de Lange syndrome.

A Selicorni1, F Lalatta, E Livini, V Briscioli, T Piguzzi, D C Bagozzi, P Mastroiacovo, G Zampino, G Gaeta, A Pugliese.   

Abstract

Brachmann-de Lange syndrome (BDLS) is a relatively common multiple congenital anomaly/mental retardation syndrome, whose cause is unknown. The clinical variability of this condition is well-known. Recently some reports suggested the possible existence of a mild BDLS phenotype. We report on 30 patients in whom a diagnosis of BDLS was made or strongly suspected in 12 different Italian hospitals. Based on clinical evaluation we divided them into two groups, classical and mild BDLS cases. We compare the clinical data of these patients and we discuss the problems which arise in trying to define clear criteria of distinction between these two groups.

Entities:  

Mesh:

Year:  1993        PMID: 8291540     DOI: 10.1002/ajmg.1320470708

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


  5 in total

Review 1.  Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrences.

Authors:  K L Russell; J E Ming; K Patel; L Jukofsky; M Magnusson; I D Krantz
Journal:  Am J Med Genet       Date:  2001-12-15

2.  Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience.

Authors:  Z A Bhuiyan; M Klein; P Hammond; A van Haeringen; M M A M Mannens; I Van Berckelaer-Onnes; R C M Hennekam
Journal:  J Med Genet       Date:  2005-10-19       Impact factor: 6.318

3.  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 4.  Cohesin and human disease.

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

Review 5.  Cornelia de Lange Syndrome: From a Disease to a Broader Spectrum.

Authors:  Angelo Selicorni; Milena Mariani; Antonella Lettieri; Valentina Massa
Journal:  Genes (Basel)       Date:  2021-07-15       Impact factor: 4.096

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.