Literature DB >> 27379896

A Rare Cause of Myoclonus: A Cupric Conundrum.

Karen M Doherty1, Joanne Shields2, Raeburn Forbes3, Moyra Gray4, Seamus Kearney1, Alexander P Maxwell2, John McKinley1.   

Abstract

A woman aged 22 years presented with a 3-year history of jerks when brushing her teeth and a tremor when carrying drinks. Examination revealed a bilateral jerky tremor, stimulus-sensitive myoclonus, and difficulty with tandem gait. Thyroid and liver function test results were normal, but she had rapidly progressive renal failure. Serum copper, ceruloplasmin, and manganese levels were normal, but her urinary copper level was elevated on 2 occasions. Pathological findings on organ biopsy prompted genetic testing to confirm the diagnosis. The differential diagnosis, tissue biopsy findings, and final genetic diagnosis are discussed.

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Year:  2016        PMID: 27379896     DOI: 10.1001/jamaneurol.2016.1553

Source DB:  PubMed          Journal:  JAMA Neurol        ISSN: 2168-6149            Impact factor:   18.302


  2 in total

1.  A Quandary of Cuprum - Wilson's Disease Disguising as Progressive Myoclonic Epilepsy.

Authors:  Monika Sachan; Suman Kushwaha; Shah Faisal Ahmad Tarfarosh; Vineet Banga; Ashutosh Gupta
Journal:  Cureus       Date:  2017-01-01

2.  Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature review.

Authors:  Burcu Atasu; Ayse Nur Ozdag Acarlı; Basar Bilgic; Betül Baykan; Erol Demir; Yasemin Ozluk; Aydin Turkmen; Ann-Kathrin Hauser; Gamze Guven; Hasmet Hanagasi; Hakan Gurvit; Murat Emre; Thomas Gasser; Ebba Lohmann
Journal:  BMC Neurol       Date:  2022-03-28       Impact factor: 2.474

  2 in total

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