Mitochondrial Encephalomyopathies [mitochondriální encefalomyopatie]
- Terms
-
Encephalomyopathies, Mitochondrial
A heterogenous group of disorders characterized by alterations of mitochondrial metabolism that result in muscle and nervous system dysfunction. These are often multisystemic and vary considerably in age at onset (usually in the first or second decade of life), distribution of affected muscles, severity, and course. (From Adams et al., Principles of Neurology, 6th ed, pp984-5)
- Annotation
- general or unspecified; prefer specifics; coordinate with specific dysfunction if pertinent
- DUI
- D017237 MeSH Browser
- CUI
- M0026153
- Previous indexing
- Brain Diseases, Metabolic (1977-1992); Mitochondria, Muscle (1977-1992); Neuromuscular Diseases (1977-1992)
- History note
- 1993
- Public note
- 1993
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 1
- CN
- congenital
- DI
- diagnosis 22
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology 4
- EP
- epidemiology 1
- EH
- ethnology
- ET
- etiology 9
- GE
- genetics 15
- HI
- history
- IM
- immunology 1
- ME
- metabolism 7
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 5
- PP
- physiopathology 6
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 5
- UR
- urine
- VE
- veterinary
- VI
- virology
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Disease MeSH Browser
Encephalocardiomyopathy, Mitochondrial, Neonatal, Due To Atp Synthase Deficiency Disease MeSH Browser
Mitochondrial encephalopathy Disease MeSH Browser