Sleep Disorders Associated with Primary Mitochondrial Diseases
Author(s) -
Ryan Ramezani,
Peter W. Stacpoole
Publication year - 2014
Publication title -
journal of clinical sleep medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 92
eISSN - 1550-9397
pISSN - 1550-9389
DOI - 10.5664/jcsm.4212
Subject(s) - medicine , sleep (system call) , mitochondrial disease , primary care , psychiatry , mitochondrial dna , family medicine , genetics , biology , computer science , gene , operating system
Primary mitochondrial diseases are caused by heritable or spontaneous mutations in nuclear DNA or mitochondrial DNA. Such pathological mutations are relatively common in humans and may lead to neurological and neuromuscular complication that could compromise normal sleep behavior. To gain insight into the potential impact of primary mitochondrial disease and sleep pathology, we reviewed the relevant English language literature in which abnormal sleep was reported in association with a mitochondrial disease.
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