| Literature DB >> 34020866 |
Georgianne L Arnold1, Jessie Yester2, Elizabeth McCracken2, Brian D Feingold2, Jerry Vockley2.
Abstract
Carnitine palmitoyl transferase II (CPT II) catalyzes the release of activated long-chain fatty acids from acylcarnitines into mitochondria for subsequent fatty acid oxidation. Depending on residual enzyme activity, deficiency of this enzyme leads to a spectrum of symptoms from early onset hypoglycemia, hyperammonemia, cardiomyopathy and death to onset of recurrent rhabdomyolysis in adolescents and young adults. We present a case of successful orthotopic heart transplantation in a patient with severe infantile onset cardiomyopathy due to CPT II deficiency identified through newborn screening. Excellent cardiac function is preserved 12 years post-transplantation; however, the patient has developed intermittent episodes of hyperammonemia and rhabdomyolysis later in childhood and early adolescence readily resolved with intravenous glucose. Successful heart transplant in this patient demonstrates the feasibility of this management option in patients with even severe forms of long chain fatty acid oxidation disorders.Entities:
Keywords: CPT2 deficiency; Cardiomyopathy; Carnitine palmitoyl transferase deficiency; Fatty acid oxidation disorder; Heart transplantation
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Year: 2021 PMID: 34020866 PMCID: PMC8899800 DOI: 10.1016/j.ymgme.2021.04.005
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797