El Síndrome de Kartagener comprende la triada de Sinusitis Crónica, Bronquiectasias y Situs Inversus, la causa primordial de esta patología es un defecto hereditario que se manifiesta durante el desarrollo embrionario producto de alteraciones en la motilidad ciliar, debido a la complejidad de su diagnóstico y su infrecuencia, es muy poca la información en la población ecuatoriana, además de la limitación tecnológica para el diagnóstico y su manejo equivoco consideramos de gran importancia el estudio del presente caso. Área de estudio: pediatría.Kartagener Syndrome is characterized by Chronic Sinusitis, Bronchiectasis and Situs Inversus, the etiology of this condition is an inherited defect that develops during the embryogenic period that involves alterations in ciliar motility, due to its difficult diagnosis and its infrequency, there is not enough information in Ecuadorian population, because to technological limitations and the difficult management, we consider important the review of this clinical case, due to its difficult diagnosis and its infrequency, there is not enough information in Ecuadorian population, because to technological limitations and the difficult management, we consider important the review of this clinical case.