Francisco Cammarata‐ScalisiYajaira BriceñoEdymar CegarraDaniela Montilla2026-03-222026-03-22201910.24875/bmhim.18000108https://doi.org/10.24875/bmhim.18000108https://andeanlibrary.org/handle/123456789/67204Clinical findings that can guide the diagnosis of this infrequent structural chromosomal alteration are highlighted, as well as the interdisciplinary medical evaluation required and adequate family genetic counseling.esMicrocephalyMedicineGynecologyPediatricsarticle