Diagnóstico prenatal: Trisomía 13 y holoprosencefalia: Reporte de un caso clínico

  • Andrés Sarmiento R.
  • Jesús A. Berdugo G
  • Guillermo Sánchez B

Resumen

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.

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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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Publicado
1992-12-31
Cómo citar
1.
Sarmiento R. A, Berdugo G JA, Sánchez B G. Diagnóstico prenatal: Trisomía 13 y holoprosencefalia: Reporte de un caso clínico. Rev. Colomb. Obstet. Ginecol. [Internet]. 31 de diciembre de 1992 [citado 23 de febrero de 2020];43(4):297-01. Disponible en: https://revista.fecolsog.org/index.php/rcog/article/view/901