Two families with the G syndrome of dysphagia, ocular hypertelorism and male genital anomalies are described. One family had a lethal case with a laryngotracheo‐oesophageal cleft, while the other showed only a relatively mild expression of the syndrome in both sexes. This wide variability and the new findings are discussed, and the importance of an early diagnosis for the successful management of severe cases is emphasized.
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