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.
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