OMENS-plus syndrome.
Indian J Pediatr
;
2005 Aug; 72(8): 707-8
Article
in English
| IMSEAR
| ID: sea-82368
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Syndrome
/
Abnormalities, Multiple
/
Female
/
Humans
/
Toes
/
Nose
/
Adolescent
/
Craniofacial Abnormalities
/
Facial Asymmetry
/
Fingers
Language:
English
Journal:
Indian J Pediatr
Year:
2005
Type:
Article
Similar
MEDLINE
...
LILACS
LIS