Volume 47, Issue 7 pp. 959-964
Article
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Brachmann-de Lange syndrome. Delineation of the clinical phenotype

M. Ireland

Corresponding Author

M. Ireland

Department of Human Genetics, University of Newcastle Upon Tyne, Newcastle upon Tyne, United Kingdom

M.R.C.P., Department of Human Genetics, University of Newcastle upon Tyne, 19/20 Claremont Place, Newcastle upon Tyne NE2 4AA, EnglandSearch for more papers by this author
D. Donnai

D. Donnai

Department of Medical Genetics, St. Mary's Hospital, Manchester, United Kingdom

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J. Burn

J. Burn

Department of Human Genetics, University of Newcastle Upon Tyne, Newcastle upon Tyne, United Kingdom

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First published: 15 November 1993
Citations: 82

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. © 1993 Wiley-Liss, Inc.

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