Progression despite replacement of a myopathic form of coenzyme Q10 defect
- PMID: 15326254
- DOI: 10.1212/01.wnl.0000134607.76780.b2
Progression despite replacement of a myopathic form of coenzyme Q10 defect
Abstract
The authors report 7 years of follow-up evaluation of a patient with coenzyme Q10 (CoQ10) deficiency. Initial symptoms of exercise intolerance and hyperlactatemia improved markedly with substitutive treatment. However, CoQ(10) supplementation did not prevent the onset of a cerebellar syndrome. A switch to idebenone treatment resulted in clinical and metabolic worsening, which disappeared with subsequent CoQ10 treatment. CoQ10 defects may cause progressive neurologic disease despite supplementation.
Similar articles
-
Cerebellar ataxia with coenzyme Q10 deficiency: diagnosis and follow-up after coenzyme Q10 supplementation.J Neurol Sci. 2006 Jul 15;246(1-2):153-8. doi: 10.1016/j.jns.2006.01.021. Epub 2006 May 3. J Neurol Sci. 2006. PMID: 16677673
-
Cerebellar ataxia and coenzyme Q10 deficiency.Neurology. 2003 Apr 8;60(7):1206-8. doi: 10.1212/01.wnl.0000055089.39373.fc. Neurology. 2003. PMID: 12682339
-
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency.Neurology. 2001 Apr 10;56(7):849-55. doi: 10.1212/wnl.56.7.849. Neurology. 2001. PMID: 11294920
-
Exercise intolerance and the mitochondrial respiratory chain.Ital J Neurol Sci. 1999 Dec;20(6):387-93. doi: 10.1007/s100720050056. Ital J Neurol Sci. 1999. PMID: 10937858 Review.
-
Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency.Cerebellum. 2007;6(2):118-22. doi: 10.1080/14734220601021700. Cerebellum. 2007. PMID: 17510911 Review.
Cited by
-
Mitochondrial Dysfunction due to Novel COQ8A Variation with Poor Response to CoQ10 Treatment: A Comprehensive Study and Review of Literatures.Cerebellum. 2024 Oct;23(5):1824-1838. doi: 10.1007/s12311-024-01671-4. Epub 2024 Mar 2. Cerebellum. 2024. PMID: 38429489 Review.
-
Redefining infantile-onset multisystem phenotypes of coenzyme Q10-deficiency in the next-generation sequencing era.J Transl Genet Genom. 2020;4:22-35. doi: 10.20517/jtgg.2020.02. Epub 2020 Apr 23. J Transl Genet Genom. 2020. PMID: 33426503 Free PMC article.
-
176th ENMC International Workshop: diagnosis and treatment of coenzyme Q₁₀ deficiency.Neuromuscul Disord. 2012 Jan;22(1):76-86. doi: 10.1016/j.nmd.2011.05.001. Epub 2011 Jul 1. Neuromuscul Disord. 2012. PMID: 21723727 Free PMC article. No abstract available.
-
Mitochondrial respiration without ubiquinone biosynthesis.Hum Mol Genet. 2013 Dec 1;22(23):4768-83. doi: 10.1093/hmg/ddt330. Epub 2013 Jul 11. Hum Mol Genet. 2013. PMID: 23847050 Free PMC article.
-
A novel COQ7 mutation causing primarily neuromuscular pathology and its treatment options.Mol Genet Metab Rep. 2022 May 5;31:100877. doi: 10.1016/j.ymgmr.2022.100877. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35782625 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources