An eleven-year history of Vanishing White Matter Disease in an adult patient with no cognitive decline and EIF2B5 mutations. A case report

Neurocase ◽  
2021 ◽  
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Lucia Trevisan ◽  
Matteo Grazzini ◽  
Annalia Cianflone ◽  
Andrea Accogli ◽  
Cinzia Finocchi ◽  
...  
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Eleonora Virgilio ◽  
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Riccardo Fornaro ◽  
Domizia Vecchio ◽  
...  

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M.A. Flores ◽  
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S.A. Messina

2012 ◽  
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Mohammad Imnul Islam ◽  
Skazimul Hoque ◽  
Md Tariqul Islam ◽  
Narayan Chandra Saha ◽  
Abdul Matin ◽  
...  

DOI: http://dx.doi.org/10.3329/bjch.v35i3.10526 Bangladesh J Child Health 2011; Vol 35 (3): 127-129


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Khadija Sonda Moalla ◽  
Nouha Farhat ◽  
Salma Sakka ◽  
Olfa Hdiji ◽  
...  

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D Prayer ◽  
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S Stöckler-Ipsiroglu

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...  

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Saroj Kumar Patnaik

AbstractA 3.5-year-old male child patient with mild developmental delay presented with history of acute onset fever, encephalopathy, and dyskinesia. The patient was investigated for common etiologies and was managed supportively. His neuroimaging was suggestive of vanishing white matter (VWM) disease which was confirmed by clinical exome sequencing. The child had an eventful hospital stay followed by near-total recovery after 4 weeks. The case attempts to sensitize readers about the current perspectives pertaining to VWM disease.


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Sedighe Nikbakht ◽  
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Nejat Mahdieh ◽  
...  

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