Article
Spectrum of movement disorders in neuroferritinopathy.
Movement disorders : official journal of the Movement Disorder Society - 1 Jan 2005
Crompton Douglas E, Chinnery Patrick F, Bates David, Walls Timothy J, Jackson Margaret J, Curtis Andrew J, Burn John
Abstract excerpt
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 progress clinically. The clinical phenotype of this disorder is highly variable with symptoms beginning in the third to sixth decades....
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