Left ventricular noncompaction and Fabry disease: two diagnoses in one heart?

Author:

Klopotowski M.,Spiewak M.,Podgorska A.,Kukuła K.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference10 articles.

1. Uribe A, Mateus H, Prieto J (2015) Identification of mutations in Colombian patients affected with Fabry disease. Gene 574:325–329

2. Azevedo O, Gaspar P, Sá Miranda C, Cunha D, Medeiros R, Lourenço A (2011) Left ventricular noncompaction in a patient with fabry disease: overdiagnosis, morphological manifestation of fabry disease or two unrelated rare conditions in the same patient. Cardiology 119:155–159

3. Martins E, Pinho T, Carpenter S et al (2014) Histopathological evidence of Fabry disease in a female patient with left ventricular noncompaction. Rev Port Cardiol 33(565):e1-6

4. Alper AT, Kaya A, Tekkesin AI, Oz A (2016) Wolff–Parkinson–White and left ventricular noncompaction in a Fabry patient: a case report. Turk Kardiyol Dern Ars 44:248–255

5. Rupp S, Felimban M, Schänzer A et al (2019) Genetic basis of hypertrophic cardiomyopathy in children. Clin Res Cardiol 108:282–289

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