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  2. Mitochondrial disease - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_disease

    Mitochondrial disease is a group of disorders ... legalize the 'three-person IVF' procedure as a treatment to fix or eliminate mitochondrial diseases that are passed ...

  3. Diabetes and deafness - Wikipedia

    en.wikipedia.org/wiki/Diabetes_and_deafness

    Diabetes and deafness (DAD) or maternally inherited diabetes and deafness (MIDD) or mitochondrial diabetes is a subtype of diabetes which is caused from a mutation in mitochondrial DNA, which consists of a circular genome. It is associated with the genes MT-TL1, MT-TE, and MT-TK. [1]

  4. Pearson syndrome - Wikipedia

    en.wikipedia.org/wiki/Pearson_syndrome

    Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure to thrive, pancreatic fibrosis with insulin-dependent diabetes and exocrine pancreatic deficiency, muscle and neurologic impairment, and, frequently, early death. It is usually fatal in infancy.

  5. Mitochondrial replacement therapy - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_replacement...

    Mitochondrial replacement therapy (MRT), sometimes called mitochondrial donation, is the replacement of mitochondria in one or more cells to prevent or ameliorate disease. MRT originated as a special form of in vitro fertilisation in which some or all of the future baby's mitochondrial DNA (mtDNA) comes from a third party.

  6. Mitochondria may trigger Crohn's disease by disrupting the ...

    www.aol.com/mitochondria-may-trigger-crohns...

    Studying mitochondrial dysfunction can help us understand the underlying mechanisms of the disease, leading to better diagnosis and treatment strategies,” Ligresti continued.

  7. MELAS syndrome - Wikipedia

    en.wikipedia.org/wiki/MELAS_syndrome

    MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes) is one of the family of mitochondrial diseases, which also include MIDD (maternally inherited diabetes and deafness), MERRF syndrome, and Leber's hereditary optic neuropathy.

  8. Mitochondrial DNA depletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA...

    Mitochondrial DNA depletion syndrome (MDS or MDDS), or Alper's disease, is any of a group of autosomal recessive disorders that cause a significant drop in mitochondrial DNA in affected tissues. Symptoms can be any combination of myopathic , hepatopathic , or encephalomyopathic . [ 1 ]

  9. Chronic progressive external ophthalmoplegia - Wikipedia

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

    CPEO is the most common manifestation of mitochondrial myopathy, occurring in an estimated two-thirds of all cases of mitochondrial myopathy. Patients typically present with ptosis (drooping eyelids). Other diseases like Graves' disease, myasthenia gravis and glioma that may cause an external ophthalmoplegia must be ruled out. [citation needed]