Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?

Citation
A. Bohring et al., Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?, AM J MED G, 85(5), 1999, pp. 438-446
Citations number
7
Categorie Soggetti
Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS
ISSN journal
01487299 → ACNP
Volume
85
Issue
5
Year of publication
1999
Pages
438 - 446
Database
ISI
SICI code
0148-7299(19990827)85:5<438:SEOOT(>2.0.ZU;2-O
Abstract
Opitz trigonocephaly (C)-like syndrome with a highly characteristic combina tion of facial anomalies including prominent metopic suture, exophthalmos, hypertelorism, cleft lip and palate, flexion deformities of the upper limbs and multiple other anomalies. We also review two very similar published ca ses formerly considered to have the C syndrome. Although there is overlap, a clinical distinction from the Opitz trigonocephaly and other syndromes se ems possible, and thus a specific causal entity may be postulated. (C) 1999 Wiley-Liss, Inc.