l carnitine deficiency radiology MRI head. A, Day 1 of PICU admission. Subtle bilateral high signal in A novel pathogenic variant in

A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features BMC Cardiovascular Disorders Springer Nature Link Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome Italian Journal of Pediatrics Springer Nature Link Brain MRI scans of the patient with primary carnitine deficiency and Download Scientific Diagram Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency a cardiac magnetic resonance study Scientific Reports Primary carnitine deficiency cardiomyopathy International Journal of Cardiology

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