Neuroferritinopathy: Pathophysiology, Presentation, Differential Diagnoses and Management
<p><strong>Background:</strong> Neuroferritinopathy (NF) is a rare autosomal dominant disease caused by mutations in the ferritin light chain 1 (<em>FTL1</em>) gene leading to abnormal excessive iron accumulation in the brain, predominantly in the basal ganglia.</p&g...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Ubiquity Press
2016-03-01
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| Series: | Tremor and Other Hyperkinetic Movements |
| Online Access: | https://tremorjournal.org/index.php/tremor/article/view/355 |