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Palliative care services in families of males with duchenne muscular dystrophy

✍ Scribed by Rebeca Arias; Jennifer Andrews; Shree Pandya; Kathleen Pettit; Christina Trout; Susan Apkon; Jane Karwoski; Christopher Cunniff; Dennis Matthews; Timothy Miller; Melinda F. Davis; F. John Meaney

Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
259 KB
Volume
44
Category
Article
ISSN
0148-639X

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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