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Tracheal occlusion in the prone position in an intubated patient with Duchenne muscular dystrophy

✍ Scribed by D. B. Rittoo; P. Morris

Book ID
108626102
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
503 KB
Volume
50
Category
Article
ISSN
0003-2409

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## Abstract One challenge in the molecular diagnosis of mitochondrial DNA (mtDNA) disorders is detection of a low percentage of mutant heteroplasmy. We report a patient who had a delayed molecular diagnosis of mitochondrial encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) syndrome