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Deficiency of "3-hydroxyacyl-CoA" dehydrogenase
Did you mean Deficiency of "3-hydroxy acyl-CoA" dehydrogenase?
- 3-hydroxyacyl-CoA dehydrogenase deficiency is an inherited condition that prevents the body from converting certain fats to energy, particularly during ...
- Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency is a rare condition that prevents the body from converting certain fats to energy, particularly ...
- ... the HADH gene have been found to cause 3-hydroxyacyl-CoA dehydrogenase deficiency. These mutations change single protein building blocks (amino ... which can lead to signs and symptoms of 3-hydroxyacyl-CoA dehydrogenase deficiency such as lack of energy (lethargy) and low ...
- ... IJlst L, Heymans HS, Wijburg FA. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: clinical presentation and follow-up of 50 patients. ... AW. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. ...
- ... hydratase beta-hydroxyacyl dehydrogenase beta-keto-reductase D-3-hydroxyacyl-CoA dehydratase D-bifunctional protein, ... Poll-The BT. Clinical and biochemical spectrum of D-bifunctional protein deficiency. Ann Neurol. 2006 Jan;59(1):92-104. ...
- ... dehydrogenase 10 MHBD MRPP2 SCHAD SDR5C1 short chain 3-hydroxyacyl-CoA dehydrogenase short chain ... 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene. ...
