Literature DB >> 16929546

Motor neuron disease associated with copper deficiency.

Conrad C Weihl1, Glenn Lopate.   

Abstract

Copper deficiency in humans is a rare cause of myeloneuropathy that usually presents with a spastic ataxic gait, hyperreflexia, and distal sensory loss similar to that seen in patients with subacute combined degeneration. We describe three copper-deficient patients, two of whom were referred with a presumptive diagnosis of amyotrophic lateral sclerosis, who had progressive asymmetric weakness or electrodiagnostic findings of proximal and distal denervation suggestive of lower motor neuron disease. Copper replacement resulted in stabilization or mild improvement in weakness. The clinical spectrum of human copper deficiency should include lower motor neuron disease in addition to a syndrome of spastic ataxia.

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Year:  2006        PMID: 16929546     DOI: 10.1002/mus.20631

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  13 in total

1.  Copper deficiency related myelopathy 40 years following a jejunoileal bypass.

Authors:  Shawn Joshi; Mitra McLarney; Benjamin Abramoff
Journal:  Spinal Cord Ser Cases       Date:  2019-12-16

2.  Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.

Authors:  Marina L Kennerson; Garth A Nicholson; Stephen G Kaler; Bartosz Kowalski; Julian F B Mercer; Jingrong Tang; Roxana M Llanos; Shannon Chu; Reinaldo I Takata; Carlos E Speck-Martins; Jonathan Baets; Leonardo Almeida-Souza; Dirk Fischer; Vincent Timmerman; Philip E Taylor; Steven S Scherer; Toby A Ferguson; Thomas D Bird; Peter De Jonghe; Shawna M E Feely; Michael E Shy; James Y Garbern
Journal:  Am J Hum Genet       Date:  2010-02-18       Impact factor: 11.025

Review 3.  ATP7A-related copper transport diseases-emerging concepts and future trends.

Authors:  Stephen G Kaler
Journal:  Nat Rev Neurol       Date:  2011-01       Impact factor: 42.937

4.  Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy.

Authors:  Ling Yi; Anthony Donsante; Marina L Kennerson; Julian F B Mercer; James Y Garbern; Stephen G Kaler
Journal:  Hum Mol Genet       Date:  2011-12-30       Impact factor: 6.150

5.  Amyotrophic lateral sclerosis: update and new developments.

Authors:  Ashley J Pratt; Elizabeth D Getzoff; J Jefferson P Perry
Journal:  Degener Neurol Neuromuscul Dis       Date:  2012-02

6.  SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency.

Authors:  Adriana P Rebelo; Dimah Saade; Claudia V Pereira; Amjad Farooq; Tyler C Huff; Lisa Abreu; Carlos T Moraes; Diana Mnatsakanova; Kathy Mathews; Hua Yang; Eric A Schon; Stephan Zuchner; Michael E Shy
Journal:  Brain       Date:  2018-03-01       Impact factor: 13.501

7.  [Copper deficiency as a treatable cause of myelopathy].

Authors:  A Jung; M Marziniak
Journal:  Nervenarzt       Date:  2008-04       Impact factor: 1.214

Review 8.  Nutritional neuropathies.

Authors:  Nancy Hammond; Yunxia Wang; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2013-05       Impact factor: 3.806

Review 9.  Copper deficiency myelopathy.

Authors:  Stephan R Jaiser; Gavin P Winston
Journal:  J Neurol       Date:  2010-03-16       Impact factor: 4.849

10.  Exogenous copper exposure causing clinical wilson disease in a patient with copper deficiency.

Authors:  Blanca C Lizaola-Mayo; Rolland C Dickson; Dora M Lam-Himlin; David M Chascsa
Journal:  BMC Gastroenterol       Date:  2021-07-08       Impact factor: 3.067

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