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Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases
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Neurology | July 27, 2012 | Volume: 79 | Issue: 9 | Pages: 878-882
An Unusual Presentation of Copper Metabolism Disorder and a Possible Connection With Niemann-Pick Type C
Goez, Helly , Jacob, Francois D. , Fealey, Robert D., Patterson, Marc C. , Ramaswamy, Vijay , Persad, Rabin, Johnson, Edward S., Yager, Jerome Y. , Patterson, Marc , Ramaswamy, Vijay
Journal of Child Neurology | January 27, 2011 | Volume: 26 | Issue: 4 | Pages: 518-521
Abnormal copper metabolism has been linked with neurological disorders, such as Wilson and Menkes disease. Another disorder causing symptoms similar to copper metabolism disorder is Niemann-Pick type C. However, a definite pathophysiological connection between Niemann-Pick type C and copper metabolism disorders has never been established. The authors present an adolescent with an unusual presentation of copper deficiency—dysarthria, ataxia, and vertical gaze paresis, without significant cognitive degeneration or pathological magnetic resonance imaging (MRI). The patient was found to carry 2 mutations in the NPC1 gene. A possible link, explaining how copper deficiency might induce the Niemann-Pick phenotype might involve overproduction of cholesterol and inhibition of acid sphingomyelinase. We suggest that copper metabolism disorders be included in the differential diagnosis for ataxia and dysarthria, even in cases with unusual presentations. Moreover, should the connection between copper and Niemann-Pick be validated, screening for copper metabolism disorders may be advisable in Niemann-Pick type C patients and vice-versa.