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Article

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene.

Pediatrics - 1 May 2006

Peddy Stacie B, Vricella Luca A, Crosson Jane E, Oswald Gretchen L, Cohn Ronald D, Cameron Duke E, Valle David, Loeys Bart L

Abstract excerpt

Here we report the first infantile case of restrictive cardiomyopathy caused by a de novo mutation of the cardiac troponin T gene. The patient presented with an apparent life-threatening event. She developed malignant arrhythmias and hemodynamic instability, requiring initial rescue support with extracorporeal membrane oxygenation, and subsequently underwent insertion of a biventricular assist device (VAD). She...

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Source

Identifiers

PMID: 16651346
DOI: 10.1542/peds.2005-2301

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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