1975/01/01 by J A Keipert
Biochemistry, Genetics and Molecular Biology · Medicine · #Hedgehog Signaling Pathway Studies #Genetic and rare skin diseases. #Cancer and Skin Lesions
paper · pdf · doi:10.1136/bjo.59.1.57
The rare congenital anomaly of euryblepharon is reported in a male infant. It is suggested that euryblepharon is due to congenital hypoplasia or absence of the palpebral and lacrimal portions of the orbicularis oculi muscle.