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1,850 Possible Causes for Mitochondrial Myopathy

  • MELAS Syndrome

    MELAS syndrome (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) is one of the classic mitochondrial encephalomyopathies with variable clinical[ncbi.nlm.nih.gov] Abstract Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare neurodegenerative disease caused by the decreased ability[ncbi.nlm.nih.gov] Among this group of disorders, the mitochondrial myopathy, encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome is one of the most frequently occurring[ncbi.nlm.nih.gov]

  • Chronic Progressive External Ophthalmoplegia

    To report the findings of cystoid macular edema in a patient with chronic progressive external ophthalmoplegia and other systemic features of mitochondrial myopathy.[ncbi.nlm.nih.gov] In conclusion, mitochondrial myopathy was definitely diagnosed.[ncbi.nlm.nih.gov] Abstract Involvement of the peripheral and central nervous systems in mitochondrial myopathy with chronic progressive external ophthalmoplegia (CPEO) has been demonstrated[ncbi.nlm.nih.gov]

  • Secondary Myopathy

    […] of Mitochondrial Myopathy (MMPOWER) RTA 408 Capsules in Patients With Mitochondrial Myopathy - MOTOR SUMMARY Mitochondrial Myopathy Dr.[mitoaction.org] Mitochondrial toxicity is a major adverse effect of nucleoside analogue treatment and can lead to myopathy.[hiv.imedpub.com] myopathies: Central core Danon Distal Malignant Hyperthermia Mitochondrial disease Myofibrillar myopathy Myopathy with tubular aggregates Myotonia: Myotonic dystrophy DM1[learningneurology.com]

  • Episodic Mitochondrial Myopathy - Optic Atrophy - Reversible Leukoencephalopathy

    Signs and symptoms of mitochondrial myopathies stem from defects of mitochondrial function.[symptoma.com] Mitochondrial myopathies are types of myopathies associated with mitochondrial disease.[en.wikipedia.org] […] patients with mitochondrial myopathies was 5% (3/60), much higher than that among general population (2%).The scoliosis in mitochondrial myopathies is usually extensive and[ncbi.nlm.nih.gov]

  • Mitochondrial Myopathy with Reversible Cytochrome C Oxidase Deficiency

    This case is an example of a rare benign infantile mitochondrial myopathy caused by CCO deficiency.[ncbi.nlm.nih.gov] Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.[adc.bmj.com] DeVivo, Mitochondrial myopathies, Annals of Neurology, 17, 6, (521-538), (2004).[doi.org]

  • Lethal Infantile Mitochondrial Myopathy

    Lethal infantile mitochondrial myopathy - How is lethal infantile mitochondrial myopathy abbreviated?[acronyms.thefreedictionary.com] LEVIM stands for "Lethal Infantile Mitochondrial Myopathy" How to abbreviate Lethal Infantile Mitochondrial Myopathy?[allacronyms.com] MalaCards integrated aliases for Mitochondrial Myopathy, Lethal, Infantile: Name: Mitochondrial Myopathy, Lethal, Infantile 58 74 Lethal Infantile Mitochondrial Myopathy 60[malacards.org]

  • Autosomal Dominant Progressive External Ophthalmoplegia Type 6

    myopathies with large mitochondrial (mt)DNA deletions.[link.springer.com] These findings may be used clinically to help diagnose mitochondrial myopathy, where a patient with peripheral neuropathy may be advised to be tested for genetic defects.[mitochondrialdiseasenews.com] Key words Mitochondrial myopathy Mitochondrial neuropathy Mitochondrial DNA deletion This is a preview of subscription content, log in to check access.[link.springer.com]

  • MERRF Syndrome

    […] associated with mitochondrial myopathies.[en.wikipedia.org] Types of Mitochondrial Myopathies Kearns-Sayre syndrome (KSS) Onset: Before age 20 Symptoms: This disorder is defined by PEO and pigmentary retinopathy, a “salt-and-pepper[mda.org] Abstract A report is given of an association of dyssynergia cerebellaris myoclonica associated with Friedreich's ataxia and mitochondrial myopathy in 2 patients.[ncbi.nlm.nih.gov]

  • Myopathic Carnitine Deficiency

    Abstract Abnormal carnitine distribution in muscle was found in 22 of 77 patients (29%), with mitochondrial myopathy.[ncbi.nlm.nih.gov] The association of fatal infantile mitochondrial myopathy, lactic acidosis and renal dysfunction was previously reported by Van Biervliet et al and appears to be a distinct[n.neurology.org] […] mellitus and deafness Maternally inherited cardiomyopathy Maternally inherited deafness Isolated mitochondrial myopathy Acute rhabdomyolysis Mitochondrial ribosomal (rRNA[neurodiffdx.com]

  • Myopathy

    What is mitochondrial myopathy?[patientslikeme.com] […] muscle (disorder) Mitochondrial myopathy Myopathy Myopathy, mitochondrial Clinical Information Acquired, familial, and congenital disorders of skeletal muscle and smooth[icd9data.com] The spectrum of exercise tolerance in mitochondrial myopathies: a study of 40 patients.[ncbi.nlm.nih.gov]

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