RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164062530 T1 Barth Syndrome (BTHS) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164062530 RD 2024/03/28 AB A genetic mitochondrial disorder with cardiomyopathy, neutropenia, skeletal myopathy with muscle weakness, 3-methylglutaconic aciduria, growth retardation, and respiratory chain dysfunction.