Diagnóstico prenatal: Trisomía 13 y holoprosencefalia: Reporte de un caso clínico
DOI:
https://doi.org/10.18597/rcog.901Palabras clave:
Holoprosencefalia, diagnóstico prenatal, trisomía 13, anomalías cráneo facialesResumen
Se presenta un caso de diagnóstico prenatal de trisomia 13 y holoprosencefalia, durante el segundo trimestre de embarazo. Se practica una revisión de la literatura existente, incluyendo criterios de diagnóstico sonográfico y aspectos genéticos asociados. Se insiste en la importancia del diagnóstico sonográfico y genético antenatal, en la determinación de un pronóstico para el manejo ante e intraparto de estos casos.
Biografía del autor/a
Andrés Sarmiento R.
M.D. Ginecobstetra. Sección de ultrasonido ginecobstétrico, Servicio médico-Caja de Previsión Social de Cundinamarca., Santafé de Bogotá. Ultrasonido ginecobstétrico, OBGYN LTDA. Santafé de Bogotá.
Jesús A. Berdugo G
M.D. V.-Genética y reproducción. Servicios Integrales de Reproducción y Genética, Santafé de Bogotá.
Guillermo Sánchez B
M.D. Ginecobstetra. Clínica David Restrepo, Santafé de Bogotá
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Esta obra está bajo una licencia internacional Creative Commons Atribución-NoComercial-SinDerivadas 4.0.
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