5C53.20Ангилал
Mitochondrial DNA depletion syndromes
Тодорхойлолт
The mitochondrial DNA (mtDNA) depletion syndrome (MDS) is a clinically heterogeneous group of mitochondrial disorders characterised by a reduction of the mtDNA copy number in affected tissues without mutations or rearrangements in the mtDNA. MDS is phenotypically heterogeneous, manifesting either as a hepatocerebral form, a myopathic form, a benign 'later-onset' myopathic form or a cardiomyopathic form.
Индексийн нэр томьёо Index terms · 21
Mitochondrial DNA depletion syndromesmtDNA depletion syndromeMitochondrial DNA depletion syndrome, hepatocerebral formNavajo neurohepatopathyAlpers-Huttenlocher syndromeProgressive neuronal degeneration of childhood with liver diseaseAlpers progressive sclerosing poliodystrophyAlpers syndromeAlpers diseaseAlpers disease or gray-matter degenerationMitochondrial DNA depletion syndrome, myopathic formMitochondrial DNA depletion syndrome, encephalomyopathic formEncephalomyopathic mitochondrial DNA depletion syndrome with methylmalonic aciduriaEncephalomyopathic mitochondrial DNA depletion syndrome with renal tubulopathyMitochondrial encephalomyopathy - aminoacidopathyBooth-Haworth-Dilling syndromeMyoneurogastrointestinal encephalopathy syndromeMitochondrial neurogastrointestinal encephalomyopathyMNGIE - [Mitochondrial neurogastrointestinal encephalomyopathy] syndromeFatal infantile lactic acidosis with methylmalonic aciduriaCongenital lactic acidosis
Монгол орчуулга хянагдаж байгаа тул англи эхийг харуулж байна. Эх сурвалж: WHO ICD-11 (MMS) · WHO сайтад харах ↗