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 :
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