Title of article
Lafora Disease: A Case Report of Progressive Myoclonic Epilepsy
Author/Authors
Delavari ، Sahar Iranian Center of Neurological Research, Neuroscience Institute - Tehran University of Medical Sciences , Olamazadeh ، Sogol Iranian Center of Neurological Research, Neuroscience Institute - Tehran University of Medical Sciences , Ameli ، Nima Iranian Center of Neurological Research, Neuroscience Institute - Tehran University of Medical Sciences , Pourghaz ، Bahareh Iranian Center of Neurological Research, Neuroscience Institute - Tehran University of Medical Sciences , Tafakhori ، Abbas Department of Neurology - Iranian Center of Neurological Research, Neuroscience Institute, Imam Khomeini Hospital Complex - Tehran University of Medical Sciences
From page
187
To page
189
Abstract
Lafora disease is a rare genetic disease caused by the accumulation of malformed glycogen products in the tissues. The disease usually manifests with idiopathic generalized tonic colonic seizures with poor response to antiepileptic drugs (AEDs). We report the case of a 19-year-old girl with the chief complaint of generalized refractory seizures, jerky movement, and cognitive deterioration with a positive history of epilepsy in her younger brother. The disease onset was at the age of 16 with jerky movement and blurred vision. She was admitted to our ward to have a long-term video EEG monitoring for further evaluation. Clinical presentation accompanied with abnormal EEG characteristics for Lafora disease, and the positive familial history were highly suggestive of Lafora disease. The disease was confirmed with genetic testing by which the mutation of EPM2A was detected.
Keywords
Lafora disease , Progressive myoclonic epilepsy , PME
Journal title
Case Reports in Clinical Practice
Journal title
Case Reports in Clinical Practice
Record number
2735979
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