Agenesis of the corpus callosum: presentation of a case

  • Patricia González Zapico Enfermera. Nidos. CAULE. SACYL.
  • Beatriz Ordás Campos Enfermera. UCI-Pediátrica. CAULE. SACYL.
  • Patricia Rodríguez Presa Enfermera. Clínica Nephrocare. Madrid. España.
  • Soraya González Martínez MIR. Pediatría. CAULE. SACYL.
  • Irene Valdés Montejo MIR. Pediatría. CAULE. SACYL.
  • María Rodrigo De la Red Enfermera. Nidos. CAULE. SACYL.
Keywords: agenesis of the corpus callosum, magnetic resonance imaging, neonate, nursing care, prenatal diagnosis

Abstract

The agenesis of the corpus callosum (ACC) is a congenital malformation that can be seen from week 20 of pregnancy with ultrasound or MRI. It is associated with visceral anormalities and brain malformations, which unravel in disorders that range from subtle to severe depending on the associated brain anomalies. The individual neurological prognosis of a fetus with ACC can not be predicted with certainty, but it is worse in the presence of associated cerebral anomalies. MRI allows confirming the suspicion and identifying additional anomalies not detected in the prenatal ultrasound so that a more precise diagnosis is possible, conditioning the obstetric management and genetic and family counseling. We present the clinical case of a newborn diagnosed with CCA in the 20th week of pregnancy and the procedure guideline is exposed. The purpose is to provide comprehensive nursing care to the newborn and parento-filial well-being during admission.

Published
2019-02-12
How to Cite
Zapico, P. G., Campos, B. O., Presa, P. R., Martínez, S. G., Montejo, I. V., & De la Red, M. R. (2019). Agenesis of the corpus callosum: presentation of a case. NURSING AND HEALTH TIMES, 1(5), 20-22. Retrieved from https://tiemposdeenfermeriaysalud.es/journal/article/view/14