Literature DB >> 8989465

Autosomal dominant inheritance of Brachmann-de Lange syndrome.

C Kozma1.   

Abstract

A mother with mild phenotype and her severely affected son, both with classic manifestations of Brachmann-de Lange syndrome (BDLS), are described. This documented mother-to-child transmission supports the hypothesis of autosomal dominant transmission with intrafamilial variability. Known cases of BDLS with autosomal dominant inheritance are reviewed. Although most cases of BDLS are sporadic, a careful evaluation of parents of affected children is important for appropriate genetic counseling.

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Year:  1996        PMID: 8989465     DOI: 10.1002/(SICI)1096-8628(19961230)66:4<445::AID-AJMG12>3.0.CO;2-U

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


  6 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.  Classical cornelia de lange syndrome.

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

3.  Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.

Authors:  I D Krantz; E Tonkin; M Smith; M Devoto; A Bottani; C Simpson; M Hofreiter; V Abraham; L Jukofsky; B P Conti; T Strachan; L Jackson
Journal:  Am J Med Genet       Date:  2001-06-15

4.  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

5.  Dosage effects of cohesin regulatory factor PDS5 on mammalian development: implications for cohesinopathies.

Authors:  Bin Zhang; Jufang Chang; Ming Fu; Jie Huang; Rakesh Kashyap; Ezequiel Salavaggione; Sanjay Jain; Shashikant Kulkarni; Kulkarni Shashikant; Matthew A Deardorff; Maria L Giovannucci Uzielli; Dale Dorsett; David C Beebe; Patrick Y Jay; Robert O Heuckeroth; Ian Krantz; Jeffrey Milbrandt
Journal:  PLoS One       Date:  2009-05-01       Impact factor: 3.240

6.  A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3.

Authors:  Emma T Tonkin; Melanie Smith; Piet Eichhorn; Sandie Jones; Burhan Imamwerdi; Susan Lindsay; Mike Jackson; Tzu-Jou Wang; Maggie Ireland; John Burn; Ian D Krantz; Philippa Carr; Tom Strachan
Journal:  Hum Genet       Date:  2004-05-27       Impact factor: 4.132

  6 in total

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