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Cardiac Amyloidosis in a Child Presenting with Syncope: The First Reported Case and a Diagnostic Dilemma
Diana Milagros Torpoco Rivera1,2, Celeste T Williams3, Peter P Karpawich4,5
1Division of Cardiology, The Children's Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI, 48201, USA. dianatorpoco1202@gmail.com.
Abstract:
Cardiac amyloidosis is a rare cause of cardiomyopathy, reported exclusively in adults. We report the first known case presenting in childhood. A 12-year-old boy presented with syncope and diagnosed with ventricular non-compaction by echocardiography. Eventual genetic testing confirmed a TTR gene mutation associated with hereditary transthyretin amyloidosis.
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