The Ohdo blepharophimosis syndrome: a third case.
Open Access
- 1 February 1991
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 28 (2) , 131-134
- https://doi.org/10.1136/jmg.28.2.131
Abstract
A patient with a syndrome consisting of blepharophimosis, simple ears, hypoplastic teeth, developmental delay, and hypotonia is described. Previous case reports are reviewed and a differential diagnosis is described. Many of the features in the subject are similar to those described in two previous reports and they constitute a distinct syndrome.Keywords
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