Nitric oxide is formed in skeletal muscle by the neuronal type nitric oxide
synthase and the signalling function of dystrophin and related compounds a
re in part mediated by nitric oxide. Duchenne muscular dystrophy, mdx mice
and patients with Becker dystrophy demonstrated neuronal type nitric oxide
synthase deficiency in muscle biopsy specimens. We have intended to find ou
t whether the plasma nitric oxide levels show any abnormality in patients w
ith Duchenne muscular dystrophy. Serum NO levels of Duchenne patients (4.19
1 +/- 2.82 mu mol/l) were significantly lower than those of the control (39
.53 +/- 19.43 mu mol/l) and cerebral palsy (77.84 +/- 21.70 mu mol/l) group
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