2,4-Dienoyl-CoA reductase deficiency
Other Names for this Disease
- Dienoyl-CoA reductase deficiency
- 2,4-alpha dienoyl-CoA reductase deficiency
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hypotonia and respiratory acidosis in infancy. This condition may be associated with the DECR1 gene and likely has an autosomal recessive pattern of inheritance.2,4-Dienoyl-CoA reductase deficiency is associated with
Last updated: 3/17/2010
- 2,4-Dienoyl-CoA reductase deficiency. Newborn Screening Coding and Terminology Guide. September 14, 2009; http://newbornscreeningcodes.nlm.nih.gov/nb/sc/condition/De-Red. Accessed 3/17/2010.
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