A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
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Lagrand, Tjerk J
McLaughlin, Laurie
Lehn, Alexander C
McLaughlin, Laurie
Lehn, Alexander C
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2022
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Abstract
Wilson's disease (WD) is a rare autosomal recessive disorder caused by homozygous or compound heterozygous mutations in the ATPase copper transporting beta (ATP7B) gene, which lead to abnormal copper deposition in different body tissues. An estimated 50% of patients report neurological or psychiatric manifestations.1
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Movement Disorders Clinical Practice
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9
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6
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Neurosciences
Science & Technology
Life Sciences & Biomedicine
Clinical Neurology
Neurosciences & Neurology
Wilson's disease
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Citation
Lagrand, TJ; McLaughlin, L; Lehn, AC, A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease, Movement Disorders Clinical Practice, 2022, 9 (6), pp. 829-831