Mitochondrial encephalomyopathy

Mitochondrial encephalomyopathy
Mitochondrial encephalomyopathy
Classification and external resources
ICD-9 277.87
MeSH D017237

A Mitochondrial encephalomyopathy is a form of encephalomyopathy that is associated with a mitochondrial disease.

Examples include MELAS and MERRF. These conditions can sometimes present together.[1][2]

KSS is sometimes included in this category,[3] but it is not included in this category in MeSH.

References



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  • Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes — Infobox Disease Name = Mitochondrial encephalomyopathy, lactic acidosis, and stroke like episodes Caption = DiseasesDB = 8254 ICD10 = ICD9 = ICDO = OMIM = 540000 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1406 MeshID = D017241… …   Wikipedia

  • mitochondrial encephalomyopathy — any of a group of diseases characterized by abnormal mitochondrial function with involvement of the central nervous system and skeletal muscle and, in most cases, lactic acidosis. Diseases in this group, which includes subacute necrotizing… …   Medical dictionary

  • Mitochondrial disease — Classification and external resources Micrograph showing ragged red fibres, a finding seen in mitochondrial diseases. Muscle biopsy. Gomori trichrome stain …   Wikipedia

  • Mitochondrial myopathy — Classification and external resources Simplified structure of a typical mitochondrion ICD 10 G …   Wikipedia

  • Mitochondrial neurogastrointestinal encephalopathy syndrome — Classification and external resources ICD 9 277.87 OMIM 603041 …   Wikipedia

  • Mitochondrial DNA — (mtDNA) is the DNA of the mitochondrion, a structure situated in the cytoplasm of the cell rather than in the nucleus (where all the other chromosomes are located). All mtDNA is inherited from the mother. There are 2 to 10 copies of the mtDNA… …   Medical dictionary

  • mitochondrial neurogastrointestinal encephalomyopathy — (MNGIE) a mitochondrial encephalomyopathy of autosomal recessive inheritance, having an onset between the second and fifth decades of life and characterized by intestinal dysmotility, ptosis, cachexia, ophthalmoplegia, peripheral neuropathy, and… …   Medical dictionary

  • DNA, mitochondrial — Mitochondrial DNA (mtDNA) is the DNA of the mitochondrion, a structure situated in the cytoplasm of the cell rather than in the nucleus (where all the other chromosomes are located). All mtDNA is inherited from the mother. There are 2 to 10… …   Medical dictionary

  • MELAS syndrome — Mitochondrial myopathy, encephalomyopathy, lactic acidosis, and stroke like episodes Classification and external resources Basal ganglia calcification, cerebellar atrophy, increased …   Wikipedia

  • mtDNA — Mitochondrial DNA (mtDNA) is the DNA of the mitochondrion, a structure situated in the cytoplasm of the cell rather than in the nucleus (where all the other chromosomes are located). All mtDNA is inherited from the mother. There are 2 to 10… …   Medical dictionary

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