Isolated succinate-CoQ reductase deficiency

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Name:
Isolated succinate-CoQ reductase deficiency
Description:
A rare, mitochondrial oxidative phosphorylation disorder characterized by a highly variable phenotype. The severe, multisystemic disease involves brain, heart, muscles, liver, kidneys, and eyes and results in death in infancy. Mildly affected individuals have only isolated cardiac or muscle involvement in the adulthood. Histochemical and biochemical analysis reveals a global reduction of succinate dehydrogenase activity.
ORPHAcode:
3208
Synonyms:
Isolated mitochondrial respiratory chain complex II deficiency
Isolated succinate dehydrogenase deficiency
Isolated succinate-coenzyme Q reductase deficiency
Isolated succinate-ubiquinone reductase deficiency
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14