OMENS-plus syndrome.

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dc.contributor.authorKapoor, Seemaen_US
dc.contributor.authorMukherjee, Sharmila Ben_US
dc.contributor.authorPaul, Rituen_US
dc.contributor.authorDhingra, Bhavnaen_US
dc.date.accessioned2005-08-01en_US
dc.date.accessioned2009-05-30T14:08:23Z
dc.date.available2005-08-01en_US
dc.date.available2009-05-30T14:08:23Z
dc.date.issued2005-08-01en_US
dc.description.abstractThe 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.en_US
dc.description.affiliationDepartment of Pediatrics, Maulana Azad Medical College & Lok Nayak Hospital, New Delhi, India.en_US
dc.identifier.citationKapoor S, Mukherjee SB, Paul R, Dhingra B. OMENS-plus syndrome. Indian Journal of Pediatrics. 2005 Aug; 72(8): 707-8en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/82368
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshAbnormalities, Multiple --diagnosisen_US
dc.subject.meshAdolescenten_US
dc.subject.meshCraniofacial Abnormalities --diagnosisen_US
dc.subject.meshFacial Asymmetry --etiologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshFingers --abnormalitiesen_US
dc.subject.meshHumansen_US
dc.subject.meshMouth Abnormalities --diagnosisen_US
dc.subject.meshNose --abnormalitiesen_US
dc.subject.meshSyndromeen_US
dc.subject.meshToes --abnormalitiesen_US
dc.titleOMENS-plus syndrome.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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