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Vol. 6 No. 3 (2012)

July 2012

Epilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia

  • Mohammad BARZEGAR
  • Mohammad SAYADNASIRI
  • Aidin TABRIZI

Iranian Journal of Child Neurology, Vol. 6 No. 3 (2012), 24 July 2012 , Page 39-43
https://doi.org/10.22037/ijcn.v6i3.3535 Published: 2012-07-17

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Abstract

How to Cite this Article: Barzegar M, Sayadnasiri M, Tabrizi A. Epilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia. Iran J Child Neurol 2012; 6(3): 39-43.

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

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Keywords:
  • Oculodentodigitalis dysplasia
  • Epilepsy
  • Spasticity
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How to Cite

BARZEGAR, M., SAYADNASIRI, M., & TABRIZI, A. (2012). Epilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia. Iranian Journal of Child Neurology, 6(3), 39–43. https://doi.org/10.22037/ijcn.v6i3.3535
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