Epilepsy as a rare neurologic manifestation of oculodentodigitalis dysplasia
Loading...
Date
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
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.
Description
Keywords
baclofen, bilirubin, carbamazepine, phenobarbital, phenytoin, timolol, anteverted nostril, article, bilirubin blood level, camptodactyly, case report, child, clinical feature, dysplasia, electroencephalogram, epilepsy, epileptic state, gait, gait disorder, genetic disorder, glaucoma, human, hyperbilirubinemia, hypoplasia, macrogyria, male, microphthalmia, neurologic examination, nuclear magnetic resonance imaging, oculodentodigitalis dysplasia, phototherapy, physical examination, physiotherapy, school child, spastic paraplegia, spasticity, tonic clonic seizure, visual acuity