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  2. Kearns–Sayre syndrome - Wikipedia

    en.wikipedia.org/wiki/KearnsSayre_syndrome

    KearnsSayre syndrome occurs spontaneously in the majority of cases. In some cases it has been shown to be inherited through mitochondrial, autosomal dominant, or autosomal recessive inheritance. There is no predilection for race or sex, and there are no known risk factors. As of 1992 there were only 226 cases reported in published literature ...

  3. Chronic progressive external ophthalmoplegia - Wikipedia

    en.wikipedia.org/wiki/Chronic_progressive...

    It is often the only feature of mitochondrial disease, in which case the term CPEO may be given as the diagnosis. In other people suffering from mitochondrial disease, CPEO occurs as part of a syndrome involving more than one part of the body, such as KearnsSayre syndrome. Occasionally CPEO may be caused by conditions other than ...

  4. Mitochondrial disease - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_disease

    Mitochondrial disease is a group of disorders caused by mitochondrial dysfunction. Mitochondria are the organelles that generate energy for the cell and are found in every cell of the human body except red blood cells. They convert the energy of food molecules into the ATP that powers most cell functions.

  5. MELAS syndrome - Wikipedia

    en.wikipedia.org/wiki/MELAS_syndrome

    The presentation of some cases is similar to that of KearnsSayre syndrome. [6] [1]Myoclonus epilepsy associated with ragged red fibers (MERRF) may be confused with MELAS as they both involve seizures, mental deterioration, and myopathy with ragged red fibers on biopsy.

  6. Cerebral folate deficiency - Wikipedia

    en.wikipedia.org/wiki/Cerebral_folate_deficiency

    If the individual has a mitochondrial disease, the FRA could be lacking adequate energy, resulting in the deficiency of folate in the brain. [12] Other causes appear to be KearnsSayre syndrome [5] and autoantibodies to the folate receptor. [6] [7] [8] Furthermore, secondary cerebral folate deficiency can develop in patients with other ...

  7. TFAM - Wikipedia

    en.wikipedia.org/wiki/TFAM

    Studies in mice have demonstrated that this gene product is required to regulate the mitochondrial genome copy number and is essential for embryonic development. A mouse model for KearnsSayre syndrome was produced when expression of this gene was eliminated by targeted disruption in heart and muscle cells. [6]

  8. Could This Overlooked Berry Be The Key To Weight Loss? - AOL

    www.aol.com/could-overlooked-berry-key-weight...

    Instead, they seemed to have better blood glucose management and fat oxidation which could, in theory, help with weight loss. However, there was no data to suggest that people actually lost weight.

  9. Mitochondrial myopathy - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_myopathy

    Mitochondrial myopathies are types of myopathies associated with mitochondrial disease. [1] Adenosine triphosphate (), the chemical used to provide energy for the cell, cannot be produced sufficiently by oxidative phosphorylation when the mitochondrion is either damaged or missing necessary enzymes or transport proteins.