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Ocular hypotelorism,submucosal cleft palate,and hypospadias: A new autosomal dominant syndrome
Authors:U. Schilbach  H.-D. Rott  Giovanni Neri  James F. Reynolds
Abstract:
A syndrome characterized by ocular hypotelorism, submucosal cleft palate, and hypospadias in males was found in ten relatives over five generations of a family. Other anomalies are blepharophimosis, upslant of palpebral fissures, and a tendency to cutaneous syndactyly of 3rd and 4th fingers as well as 2nd and 3rd toes. Autosomal dominant inheritance is likely.
Keywords:Facio-genital syndrome  genital anomalies  hypotelorism  autosomal dominant syndrome
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