Respiratory Chain Defects May Present Only with Hypoglycemia

Hypoglycemia occasionally results from oxidative phosphorylation deficiency, associated with liver failure. Conversely, in some cases of respiratory chain defect, the impairment in glucose metabolism occurs with normal hepatic function. The mechanism for this hypoglycemia remains poorly understood....

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Veröffentlicht in:	The journal of clinical endocrinology and metabolism 2005-06, Vol.90 (6), p.3780-3785
Hauptverfasser:	Mochel, Fanny, Slama, Abdelhamid, Touati, Guy, Desguerre, Isabelle, Giurgea, Irina, Rabier, Daniel, Brivet, Michele, Rustin, Pierre, Saudubray, Jean-Marie, DeLonlay, Pascale
Format:	Artikel
Sprache:	eng
Schlagworte:	Acyl-CoA Dehydrogenase, Long-Chain Acyl-CoA Dehydrogenase, Long-Chain - deficiency Amino Acids Amino Acids - blood Biological and medical sciences Child Child, Preschool Consanguinity Endocrinology and metabolism Endocrinopathies Female Fundamental and applied biological sciences. Psychology Human health and pathology Humans Hypoglycemia Hypoglycemia - etiology Infant Life Sciences Medical sciences Mitochondria, Liver Mitochondria, Liver - enzymology Mitochondria, Liver - genetics Mitochondria, Muscle Mitochondria, Muscle - enzymology Mitochondria, Muscle - genetics Oxidative Phosphorylation Pediatrics Vertebrates: endocrinology
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