Heart Transplantation for TANGO2-Related Metabolic Encephalopathy and Arrhythmia Syndrome-Associated Cardiomyopathy

Circ Genom Precis Med. 2020 Aug;13(4):e002928. doi: 10.1161/CIRCGEN.120.002928. Epub 2020 Jun 11.

Authors

Joshua K Meisner¹, Elizabeth G Ames², Ayesha Ahmad², Ming-Sing Si³, Kurt R Schumacher¹, Heang M Lim¹, Raja Rabah⁴, David M Peng¹

Affiliations

¹ Division of Pediatric Cardiology (J.K.M., K.R.S., H.M.L., D.M.P.), University of Michigan, Ann Arbor.
² Division of Pediatric Genetics, Metabolism and Genomic Medicine (E.G.A., A.A.), University of Michigan, Ann Arbor.
³ Division of Pediatric Cardiovascular Surgery (M.-S.S.), University of Michigan, Ann Arbor.
⁴ Division of Pediatric and Perinatal Pathology (R.R.), University of Michigan, Ann Arbor.

PMID: 32527145
DOI: 10.1161/CIRCGEN.120.002928

No abstract available

Keywords: 22q11 deletion syndrome; cardiomyopathy; heart transplantation; metabolism, inborn errors; rhabdomyolysis; torsades de pointes.

Publication types

Case Reports
Letter

MeSH terms

Arrhythmias, Cardiac / complications
Arrhythmias, Cardiac / diagnosis
Arrhythmias, Cardiac / genetics*
Aryl Hydrocarbon Receptor Nuclear Translocator / genetics*
Brain Diseases, Metabolic / diagnosis
Brain Diseases, Metabolic / genetics*
Cardiomyopathies / diagnosis*
Cardiomyopathies / etiology
Cardiomyopathies / therapy
Child
Chromosomes, Human, Pair 22 / genetics
Female
Gene Deletion
Heart Transplantation*
Humans

Substances

ARNT protein, human
Aryl Hydrocarbon Receptor Nuclear Translocator