The Stoll-Kieny-Dott syndrome or Robin sequence consists of mandibular hypoplasia, glossoptosis, and a posterior cleft palate. This complex disorder can be seen alone or as a symptom of numerous other syndromes (Williams et al. 1981). The majority of cases are occasional occurrences. A multiple congenital abnormality (MCA) syndrome that has not previously been identified appears to be represented by the association of this sequence with ventricular extrasystoles and peromelia in several relatives (Stoll et al. 1992).