Please use this identifier to cite or link to this item: http://imsear.hellis.org/handle/123456789/82368
Title: OMENS-plus syndrome.
Authors: Kapoor, Seema
Mukherjee, Sharmila B
Paul, Ritu
Dhingra, Bhavna
Issue Date: 1-Aug-2005
Citation: Kapoor S, Mukherjee SB, Paul R, Dhingra B. OMENS-plus syndrome. Indian Journal of Pediatrics. 2005 Aug; 72(8): 707-8
Abstract: The 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.
URI: http://imsear.hellis.org/handle/123456789/82368
Appears in Collections:Indian Journal of Pediatrics

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