Síndrome de Apert con agenesia renal, ¿una rara asociación? (Apert syndrome and unilateral renal agenesis, a rare association?)

Summary a pert syndrome is a genetic disorder of autosomal dominant transmission. It is characterized by craniofacial malformations that cause craniosynostosis, hypoplasia of the middle third of the face and severe symmetrical syndactyly of hands and feet. We describe this disease in a newborn, in whom unilateral renal agenesis was also observed, which exceptionally has been associated with the syndrome described, and review the medical literature on the topic.