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Yang, C. 3-hydroxyacyl-CoA Dehydrogenase Deficiency. Encyclopedia. Available online: https://encyclopedia.pub/entry/4146 (accessed on 27 September 2026).
Yang C. 3-hydroxyacyl-CoA Dehydrogenase Deficiency. Encyclopedia. Available at: https://encyclopedia.pub/entry/4146. Accessed September 27, 2026.
Yang, Catherine. "3-hydroxyacyl-CoA Dehydrogenase Deficiency" Encyclopedia, https://encyclopedia.pub/entry/4146 (accessed September 27, 2026).
Yang, C. (2020, December 23). 3-hydroxyacyl-CoA Dehydrogenase Deficiency. In Encyclopedia. https://encyclopedia.pub/entry/4146
Yang, Catherine. "3-hydroxyacyl-CoA Dehydrogenase Deficiency." Encyclopedia. Web. 23 December, 2020.
3-hydroxyacyl-CoA Dehydrogenase Deficiency
Edit
This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/3-hydroxyacyl-coa-dehydrogenase-deficiency

3-hydroxyacyl-CoA dehydrogenase deficiency is an inherited condition that prevents the body from converting certain fats to energy, particularly during prolonged periods without food (fasting).

genetic conditions

References

  1. Bennett MJ, Russell LK, Tokunaga C, Narayan SB, Tan L, Seegmiller A, BoriackRL, Strauss AW. Reye-like syndrome resulting from novel missense mutations inmitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. MolGenet Metab. 2006 Sep-Oct;89(1-2):74-9.
  2. Bennett MJ, Spotswood SD, Ross KF, Comfort S, Koonce R, Boriack RL, IJlst L,Wanders RJ. Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenasedeficiency: clinical, biochemical, and pathological studies on three subjectswith this recently identified disorder of mitochondrial beta-oxidation. PediatrDev Pathol. 1999 Jul-Aug;2(4):337-45.
  3. Filling C, Keller B, Hirschberg D, Marschall HU, Jörnvall H, Bennett MJ,Oppermann U. Role of short-chain hydroxyacyl CoA dehydrogenases in SCHADdeficiency. Biochem Biophys Res Commun. 2008 Mar 28;368(1):6-11.
  4. Rinaldo P, Matern D, Bennett MJ. Fatty acid oxidation disorders. Annu RevPhysiol. 2002;64:477-502. Review.
  5. Treacy EP, Lambert DM, Barnes R, Boriack RL, Vockley J, O'brien LK, Jones PM, Bennett MJ. Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiencypresenting as unexpected infant death: A family study. J Pediatr. 2000Aug;137(2):257-9.
  6. Yang SY, He XY, Schulz H. 3-Hydroxyacyl-CoA dehydrogenase and short chain3-hydroxyacyl-CoA dehydrogenase in human health and disease. FEBS J. 2005Oct;272(19):4874-83. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Catherine Yang
View Times: 862
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 23 Dec 2020
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