@article{IR,
      author = {Saini, Ajesh and Gonzales-De Alba, Cesar},
      url = {http://digitalcollections.ohsu.edu/record/8416},
      title = {Sudden cardiac death in young adults with long-chain  3-hydroxyacyl coa dehydrogenase deficiency (LCHADD)},
      publisher = {Oregon Health and Science University},
      abstract = {Long-chain 3-Hydroxyacyl CoA Dehydrogenase Deficiency  (LCHADD) is an autosomal recessive defect in fatty acid  oxidation that presents with hypoketotic hypoglycemia  and/or hypertrophic cardiomyopathy in infancy, and  recurrent rhabdomyolysis in adolescence, however, sudden  cardiac death has not been a previously reported  complication of LCHADD. We have conducted a case review  study comparing young adult LCHADD patients who have  experienced sudden cardiac arrest events (n=5) to similar  patients who have not (n=5) for the purpose of evaluating  associated cardiac risk factors.},
      number = {IR},
      doi = {https://doi.org/10.6083/cj82k793z},
      recid = {8416},
      address = {2020},
}