Fatal case of mitochondrial DNA depletion with severe asphyxia in a newborn

Pediatr Int. 2011 Apr;53(2):240-2. doi: 10.1111/j.1442-200X.2010.03183.x.

Authors

Yuya Nakano¹, Kei Murayama, Tomkoko Tsuruoka, Madoka Aizawa, Hironori Nagasaka, Hiroshi Horie, Akira Ohtake, Kayoko Saitou

Affiliation

¹ Department of Pediatrics, Showa University School of Medicine, Department of Genetics, Tokyo Women's Medical University, Tokyo, Japan. nakano-yt@tulip.sannet.ne.jp

PMID: 21501307
DOI: 10.1111/j.1442-200X.2010.03183.x

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Asphyxia Neonatorum / genetics*
Bradycardia / genetics
DNA, Mitochondrial
Electron Transport Complex I / metabolism
Humans
Infant, Newborn
Male
Mitochondrial Diseases / genetics*
Muscle, Skeletal / metabolism
Syndrome

Substances

DNA, Mitochondrial
Electron Transport Complex I