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Indian J Ophthalmol ; 2009 Sept; 57(5): 387-389
Article de Anglais | IMSEAR | ID: sea-135983

RÉSUMÉ

Delleman Oorthuys syndrome (oculocerebrocutaneous syndrome) is a rare, congenital sporadic disorder affecting the skin and central nervous system. We present the case of a one-month-old male who presented with an orbital cyst in the left eye since birth along with other manifestations of this syndrome. The manifestations of this syndrome resemble other developmental disorders like Goldenhar and Goltz syndrome. Conservative management of the orbital cyst in these cases have been described. The need to diagnose this rare congenital anomaly with cerebral malformations as a separate entity is crucial in the management of these children.


Sujet(s)
Malformations multiples/diagnostic , Diagnostic différentiel , Malformations oculaires/diagnostic , Études de suivi , Humains , Nouveau-né , Mâle , Malformations du système nerveux/diagnostic , Malformations cutanées/diagnostic , Syndrome , Tomodensitométrie
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