Caso clínico
Diagnóstico prenatal de trisomía 21 y holoprosencefalia semilobar. Presentación de una asociación poco frecuente
Prenatal diagnosis of trisomy 21 and semilobar holoprosencephaly. Presentation of a rare association
J.H. Jiméneza,b,
, D. Galloc, H. Pachajoab, E.F. Carrilloa,b, R. Cifuentesc, A. Valderramaa,b
Autor para correspondencia
a Instituto de Investigaciones Biomédicas (IIB), Universidad Libre, Seccional Cali, Cali, Colombia
b Área de Ciencias Básicas, Facultad de Ciencias de la Salud, Universidad Libre, Seccional Cali, Cali, Colombia
c Grupo de Investigación de Ginecología y Obstetricia (GIGYO), Universidad Libre, Seccional Cali, Cali, Colombia
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