OMENS-plus syndrome.
Indian J Pediatr
;
2005 Aug; 72(8): 707-8
Artigo
em Inglês
| 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.
Texto completo:
DisponíveL
Índice:
IMSEAR (Sudeste Asiático)
Assunto principal:
Síndrome
/
Anormalidades Múltiplas
/
Feminino
/
Humanos
/
Dedos do Pé
/
Nariz
/
Adolescente
/
Anormalidades Craniofaciais
/
Assimetria Facial
/
Dedos
Idioma:
Inglês
Revista:
Indian J Pediatr
Ano de publicação:
2005
Tipo de documento:
Artigo
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