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Article

Infantile dilated cardiomyopathy caused by RPL3L gene mutation: A case report.

The Journal of international medical research - 1 May 2026

Mai Biwei, Lei Zhixian, Qin Shanqing, Yang Guidan, Zhu Naiyun, Lin Wanqian

Abstract excerpt

Ribosomal protein L3-like gene mutations have been implicated in early-onset severe dilated cardiomyopathy (OMIM #115200). This report describes an infant with dilated cardiomyopathy resulting from RPL3L gene mutations. A 2-month-old girl was admitted in June 2022 with poor appetite, breathlessness, and lethargy. Her brother had succumbed to fulminant cardiomyopathy and heart failure at the same age. Cardiac...

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Identifiers

PMID: 42156347
DOI: 10.1177/03000605261447152
PMCID: PMC13187370

Genes

RPL3L

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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