Title of article
Epilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia
Author/Authors
Barzegar-Jalali، Mohammad نويسنده , , SAYADNASIR، Mohammad نويسنده Assistant professor of Neurology, Department of Neurology, Qazvin University of Medical Sciences, Qazvin, Iran , , TABRIZI، Aidin نويسنده Pediarician, Pediatric Health Research Center, Tabriz University of Medical Sciences,Tabriz, Iran ,
Issue Information
فصلنامه با شماره پیاپی - سال 2012
Pages
5
From page
39
To page
43
Abstract
Oculodentodigitalis dysplasia (ODDD) is an extremely rare inherited disorderinvolving the development of the face, eyes, teeth and limbs. In addition,some patients develop neurological problems mostly a spastic paraparesisassociated with white matter abnormalities on magnetic resonance imaging.This report describes a patient with epilepsy, a rare neurologic manifestationof this syndrome.
References
Journal title
Iranian Journal of Child Neurology (IJCN)
Serial Year
2012
Journal title
Iranian Journal of Child Neurology (IJCN)
Record number
681511
Link To Document