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Inicio Medicina Clínica (English Edition) Cornelia de Lange syndrome: Ventricular size and function in six children withou...
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Vol. 154. Issue 2.
Pages 67-68 (January 2020)
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Vol. 154. Issue 2.
Pages 67-68 (January 2020)
Scientific letter
DOI: 10.1016/j.medcle.2018.10.036
Cornelia de Lange syndrome: Ventricular size and function in six children without congenital heart defects
Síndrome Cornelia de Lange: tamaño y función ventricular en seis casos sin cardiopatía congénita
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Ariadna Ayerza-Casasa,b, Beatriz Puisac-Uriolb, Juan Pie-Justeb,
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juanpie@unizar.es

Corresponding author.
a Unidad de Cardiología Pediátrica, Servicio de Pediatría, Hospital Universitario Miguel Servet, Zaragoza, Spain
b Unidad de Genética Clínica y Genómica Funcional, Departamento de Farmacología-Fisiología, Facultad de Medicina, Universidad de Zaragoza, Instituto de Investigación Sanitaria (IIS)-Aragón, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER)-GCV02, Zaragoza, Spain
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Table 1. Ventricular function data obtained in the echocardiography of children with Cornelia de Lange syndrome.

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