BLEPHAROLABIOANAL SYNDROME

A previously unreported syndrome of congenital craniofacial and anorec tal anomalies affecting a woman and her two daughters is described. Fe atures include bilateral cleft lip, cleft palate, bilateral upper and lower lid lag, and imperforate anus. The findings are consistent with an autosomal dominant pattern of inheritance. There were no identifiab le intrauterine fetal insults. A detailed description of these anomali es, the subsequent surgical corrections, and a discussion of previousl y unreported syndromes with isolated features are the subject of this report.