Paper Information

Journal:   IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)   SUMMER 2012 , Volume 6 , Number 3; Page(s) 39 To 43.
 
Paper: 

EPILEPSY AS A RARE NEUROLOGIC MANIFESTATION OF OCULODENTODIGITALIS DYSPLASIA

 
 
Author(s):  BARZEGAR MOHAMMAD*, SAYADNASIRI MOHAMMAD, TABRIZI AIDIN
 
* PEDIATRIC HEALTH RESEARCH CENTER, TABRIZ UNIVERSITY OF MEDICAL SCIENCES, TABRIZ, IRAN
 
Abstract: 

Oculodentodigitalis dysplasia (ODDD) is an extremely rare inherited disorder involving the development of the face, eyes, teeth and limbs. In addition, some patients develop neurological problems mostly a spastic paraparesis associated with white matter abnormalities on magnetic resonance imaging. This report describes a patient with epilepsy, a rare neurologic manifestation of this syndrome.

 
Keyword(s): OCULODENTODIGITALIS DYSPLASIA, EPILEPSY, SPASTICITY
 
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