Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0033377 (
prolapse
)
11,717
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
A 33-month-old boy with recurrent stroke-like episodes had angiographic features characteristic of moyamoya syndrome. Mitochondrial encephalomyopathy was suspected because of lactic acidosis and
ptosis
. Studies of oxidative metabolism on isolated skeletal muscle mitochondria revealed impairment of
NADH-coenzyme Q reductase
activity. Mitochondrial metabolic disorders may cause moyamoya syndrome when other known associated factors are absent.
...
PMID:Impaired NADH-CoQ reductase activity in a child with moyamoya syndrome. 314 83
