Right coronary artery originated from left coronary sinus associated with children hypertrophic cardiomyopathy: report of two cases and literature review.

Meng Xu, Tingting Xiao, Cuilan Hou, Xunwei Jiang, Li Zhang, Lijian Xie

Abstract readCase Reports

In one paragraph

Article in Open medicine (Warsaw, Poland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed

–field-weighted citation impact

1 · What the graph read from it

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Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Meng XuDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.ORCID https://orcid.org/0000-0003-2432-4942

Tingting XiaoDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.ORCID https://orcid.org/0000-0001-7311-4496

Cuilan HouDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Xunwei JiangDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.ORCID https://orcid.org/0000-0002-6449-8632

Li ZhangDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.ORCID https://orcid.org/0009-0008-9064-8922

Lijian XieDepartment of Cardiology, Shanghai Children's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Coronary artery anomalies are rare both in coronary angiogram and computed tomography angiography. Hypertrophic cardiomyopathy (HCM) is the most frequent inherited cardiac disease. The phenotype of HCM associated with anomalous coronary origin is not commonly seen especially in children. Case presentation: We describe a case series of two children with HCM combined right coronary artery (RCA) originated from left coronary sinus. Case 1 was a 9-month-old female with Conclusions: HCM coexisted with anomalous origin of RCA has different clinical presentation, and it maybe due to different gene mutation.

Indexed as

coronary arteryhypertrophic cardiomyopathymutationMYBPC3TTN

Identifiers

PMID41726140

DOI10.1515/med-2025-1287

PMCPMC12917601

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.