Literature DB >> 6650570

Definition and diagnosis of the Brachmann-De Lange syndrome.

M Preus, A P Rex.   

Abstract

We have classified patients referred for suspicion of the Brachmann-De Lange syndrome (BDLS) into two groups using techniques of numerical taxonomy. Patients with the syndrome share an array of abnormal characteristics, and those without it have different abnormal characteristics. A group of 30 characters that best distinguish the two groups of patients was used to construct a diagnostic index. The index score is expected to divide 99% of patients into those with and without the syndrome, leaving 1% in a "zone of doubt." All 46 patients used to construct the index and 16 new patients had scores in either the BDLS or non-BDLS range and none were in the zone of doubt. A previously published index using metacarpal-phalangeal measurements, although less discriminatory, confirmed our findings in 84% of 25 patients tested, the remainder having scores in the zone of doubt for that index.

Entities:  

Mesh:

Year:  1983        PMID: 6650570     DOI: 10.1002/ajmg.1320160303

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


  8 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.  Cornelia de Lange syndrome associated with Wilms' tumour and infantile haemangioendothelioma of the liver: report of two autopsy cases.

Authors:  M Maruiwa; Y Nakamura; K Motomura; T Murakami; M Kojiro; M Kato; M Morimatsu; S Fukuda; T Hashimoto
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1988

3.  Brachmann-de Lange syndrome in sibs.

Authors:  K K Naguib; A S Teebi; S A Al-Awadi; M J Marafie
Journal:  J Med Genet       Date:  1987-10       Impact factor: 6.318

4.  Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey.

Authors:  Sarika Rohatgi; Dinah Clark; Antonie D Kline; Laird G Jackson; Juan Pie; Victoria Siu; Feliciano J Ramos; Ian D Krantz; Matthew A Deardorff
Journal:  Am J Med Genet A       Date:  2010-07       Impact factor: 2.802

5.  A Case Report of Cornelia De Lange Syndrome in Northern Iran; A Clinical and Diagnostic Study.

Authors:  Seyyed-Mohsen Hosseininejad; Behnaz Bazrafshan; Ehsan Alaee
Journal:  J Clin Diagn Res       Date:  2016-02-01

6.  A case of Cornelia de Lange syndrome from Sudan.

Authors:  Mona Ellaithi; David Gisselsson; Therese Nilsson; Atif Elagib; Imad Fadl-Elmula; Mashair Abdelgadir
Journal:  BMC Pediatr       Date:  2007-01-29       Impact factor: 2.125

7.  A newborn with Cornelia de Lange syndrome: a case report.

Authors:  Hakan Uzun; Dursun Ali Senses; Munevver Uluba; Kenan Kocabay
Journal:  Cases J       Date:  2008-11-19

Review 8.  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

  8 in total

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