Kapoor, SeemaMukherjee, Sharmila BPaul, RituDhingra, Bhavna2005-08-012009-05-302005-08-012009-05-302005-08-01Kapoor S, Mukherjee SB, Paul R, Dhingra B. OMENS-plus syndrome. Indian Journal of Pediatrics. 2005 Aug; 72(8): 707-8http://imsear.searo.who.int/handle/123456789/82368The OMENS syndrome involves craniofacial maldevelopment of the orbit, ear cranial nerve and soft tissue, while OMENS-plus syndrome also includes extracraniofacial anomalies. These may be skeletal, cardiovascular, gastrointestinal, pulmonary, renal and central nervous system malformations. A fourteen-year-old girl presented with hemifacial microsomia, digital abnormalities and pancreatitis. She was diagnosed as O1M2E0N2S1--plus syndrome. Investigations revealed a type Ic choledochal cyst. The latter has not been reported as a gastrointestinal association earlier in literature to the best of the authors' knowledge.engAbnormalities, Multiple --diagnosisAdolescentCraniofacial Abnormalities --diagnosisFacial Asymmetry --etiologyFemaleFingers --abnormalitiesHumansMouth Abnormalities --diagnosisNose --abnormalitiesSyndromeToes --abnormalitiesCase Reports