Roberts syndrome is a rare genetic disorder characterized by pre- and postnatal growth retardation, symmetrical limb defects and craniofacial anomalies. A report is given on a 5 year old male child showing the following anomalies; bilateral aplasia of distal humerus, radius, ulnar and 5th mid-phalanx of hand, cleft palate, hypertelorism and craniosynostosis, pronated foot with genu valgus. We report one case of Roberts syndrome with review of literature. (J Korean Acad Rehab Med 2002; 26: 352-354)
