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Myopathy with abnormal lipid metabolism
- Mitochondrial DNA Depletion Syndrome (Alpers' Disease)
(National Institute of Neurological Disorders and Stroke)
Mitochondrial Diseases/Specifics ... Mitochondrial Diseases ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics - Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases ... Mitochondrial disorders are caused by defects in mitochondria, ...
- Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... Muscle Disorders/Specifics ... Muscle Disorders ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders
- Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Institute of Neurological ...
- ... II 3-methylglutaconic aciduria type 2 BTHS Cardioskeletal myopathy with neutropenia and abnormal mitochondria DNAJC19 defect MGA type 2 MGA type ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as ... Epub 2013 Jan 8. Citation on PubMed
- Muscle Disorders/Reference Desk ... Muscle Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Health care ...
- Neuromuscular Disorders/Reference Desk ... Neuromuscular Disorders ... Muscle Disorders/Reference Desk ... Muscle Disorders ... National Institute of Neurological Disorders ...
- ... cells. Tafazzin is involved in altering a fat (lipid) called cardiolipin, which plays critical roles in the ... FM. The enigmatic role of tafazzin in cardiolipin metabolism. Biochim Biophys Acta. 2009 Oct;1788(10):2003- ...