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Mitochondrial disease can manifest in many different ways [1] whether in children [2] or adults. [3] Examples of mitochondrial diseases include: Mitochondrial myopathy [2] [3] Maternally inherited diabetes mellitus and deafness (MIDD) [4] While diabetes mellitus and deafness can be found together for other reasons, at an early age this ...
Pages in category "Mitochondrial diseases" The following 25 pages are in this category, out of 25 total. This list may not reflect recent changes. ...
Adult-onset immunodeficiency syndrome; Advanced sleep phase disorder; Aerotoxic syndrome; Afferent loop syndrome; Aicardi syndrome; Aicardi–Goutières syndrome; AIDS dysmorphic syndrome; Al-Raqad syndrome; Alagille syndrome; Albinism–deafness syndrome; Alcohol withdrawal syndrome; Alezzandrini syndrome; Alice in Wonderland syndrome; Alien ...
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 ]
Mitochondrial cytopathy (generic term) Mitochondrial diseases of nuclear origin; Mitochondrial diseases, clinically undefinite; Mitochondrial disease; Mitochondrial encephalomyopathy aminoacidopathy; Mitochondrial genetic disorders; Mitochondrial myopathy lactic acidosis; Mitochondrial myopathy-encephalopathy-lactic acidosis; Mitochondrial ...
Mitochondrial myopathy literally means mitochondrial muscle disease, muscle disease caused by mitochondrial dysfunction. The mitochondrion is the primary producer of energy in nearly all cells throughout the body. The exception is mature erythrocytes (red blood cells), so that they do not use up the oxygen that they carry.
Mitochondrial encephalopathy is an umbrella term encompassing a variety of disorder that all result from disruptions in mitochondrial function. An overwhelming majority of genes that play a role in mitochondrial function are present within the nuclear DNA, with the remainder (13 proteins, 22 tRNAs, and 2 rRNAs) being encoded by the ...
Mitochondria. Pearson syndrome is a mitochondrial disease caused by a deletion in mitochondrial DNA (mtDNA). [3] An mtDNA is genetic material contained in the cellular organelle called the mitochondria. Depending on the tissue type, each cell contains hundreds to thousands of mitochondria. There are 2–10 mtDNA molecules in each mitochondrion.