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Clinical Spectrum of Movement Disorders after Stroke in Childhood and Adulthood

✍ Scribed by Béjot, Yannick; Giroud, Maurice; Moreau, Thibault; Benatru, Isabelle

Book ID
111966826
Publisher
S. Karger AG
Year
2012
Tongue
English
Weight
163 KB
Volume
68
Category
Article
ISSN
0014-3022

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## Abstract Neuroferritinopathy is a recently recognized, dominantly inherited movement disorder caused by a mutation of the ferritin light chain gene. We present video case reports of 4 individuals with neuroferritinopathy chosen to illustrate how this disorder can present and subsequently progres