Succinic acidaemia (Q102307): Difference between revisions

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Latest revision as of 19:14, 16 August 2026

Succinic acidemia has been described in two female sibs (the first sib died shortly after birth and the other was diagnosed at the fetal stage). The first sib also had lactic acidosis and respiratory distress. This is presumably an autosomal recessive disorder. NADH-cytochrome C reductase activity was significantly low in both cases and NADH-ferricyanide reductase activity was also low in the fetal case, suggesting a complex I deficiency of the electron transport system in the mitochondrial membrane.

Language	Label	Description	Also known as
default for all languages	ID_1257937011
English	Succinic acidaemia	Succinic acidemia has been described in two female sibs (the first sib died shortly after birth and the other was diagnosed at the fetal stage). The first sib also had lactic acidosis and respiratory distress. This is presumably an autosomal recessive disorder. NADH-cytochrome C reductase activity was significantly low in both cases and NADH-ferricyanide reductase activity was also low in the fetal case, suggesting a complex I deficiency of the electron transport system in the mitochondrial membrane.