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Gastrointestinal and hepatic manifestations of mitochondrial disorders

14 May 2013

Abstract excerpt

Inherited defects of oxidative phosphorylation lead to heterogeneous, often multisystem, mitochondrial diseases. This review highlights those mitochondrial syndromes with prominent gastrointestinal and hepatic symptoms, categorised according to underlying disease mechanism. Mitochondrial encephalopathies with major gastrointestinal involvement include mitochondrial neurogastrointestinal encephalopathy and...

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PMID: 23674168
DOI: 10.1007/s10545-013-9614-2

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