Non compaction cardiomyopathy and familial adenomatous polyposis. An unknown phenotypic trait? A case report

Authors

  • Luis Flores Sánchez de León Cardiología. Hospital Universitario La Princesa. Madrid. España. https://orcid.org/0009-0003-1742-0677
  • Lourdes Dominguez Arganda Cardiología. Hospital Universitario La Princesa. Madrid. España.
  • Kembly Webb Webb Cardiología. Hospital Dr. Rafael Ángel Calderón Guardia. San José. Costa Rica.
  • Susana Hernández Muñiz Radiología. Hospital Universitario La Princesa. Madrid. España.
  • Luis Jesús Jiménez Borreguero Cardiología. Hospital Universitario La Princesa. Madrid. España.

DOI:

https://doi.org/10.37615/retic.v8n3a4

Keywords:

cardiomyopathies, excessive trabeculation of the left ventricle, Gardner syndrome

Abstract

We present a case report of a young patient with excessive trabeculation of the left ventricle and familial polyposis syndrome. The existence of both pathologies so rarely prevalent in a single individual could suggest the existence of a previously unknown relationship between the two.

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References

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Published

2025-12-16

How to Cite

1.
Flores Sánchez de León L, Dominguez Arganda L, Webb Webb K, Hernández Muñiz S, Jiménez Borreguero LJ. Non compaction cardiomyopathy and familial adenomatous polyposis. An unknown phenotypic trait? A case report. Rev Ecocardiogr Pract Otras Tec Imag Card (RETIC) [Internet]. 2025 Dec. 16 [cited 2026 Jan. 2];8(3):21-5. Available from: https://imagenretic.org/RevEcocarPract/article/view/746