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.
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CITATION STYLE
APA
Biesecker, L. G. (1991). The Ohdo blepharophimosis syndrome: A third case. Journal of Medical Genetics, 28(2), 131–134. https://doi.org/10.1136/jmg.28.2.131
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