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 CASE REPORTS
Year : 2018  |  Volume : 13  |  Issue : 3  |  Page : 340-342

A rare cause of refractory epilepsy: Posterior periventricular nodular heterotopia


1 Division of Pediatric Neurology, Department of Pediatrics University of Mersin School of Medicine, Mersin, Turkey
2 Department of Radiology, University of Mersin School of Medicine, Mersin, Turkey

Correspondence Address:
Dr. Meltem C Direk
Division of Pediatric Neurology, Department of Pediatrics, University of Mersin School of Medicine, 34 Cadde, Ciftlikkoy Kampusu 33343, Mersin
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/JPN.JPN_178_17

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A 15-year-old male patient presented to our outpatient clinic with drug-resistant seizures. Magnetic resonance imaging of the brain showed bilateral posterior nodular heterotopia and left cerebellar dysgenesis. The patient was diagnosed with cortical developmental malformation and medically refractory epilepsy. The filamin A gene mutation was negative. Posterior periventricular nodular heterotopia is a rarer and a more different entity from classical periventricular nodular heterotopia with no gender difference and negative filamin A gene mutation. There is a limited number of case studies on posterior periventricular heterotopia. Therefore, this patient was presented to emphasize that epilepsy may be more refractory to treatment, and central congenital abnormalities including posterior fossa abnormalities are more frequent in patients with posterior periventricular nodular heterotopia.






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