Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia.
Sevil DorumCengiz HavalıPublished in: Pediatrics international : official journal of the Japan Pediatric Society (2021)
In this study, we describe the 2 patients with hyperargininemia who carried 2 novel variations of the ARG1 gene. Also, we present a patient with normal neurodevelopment who was diagnosed prenatally and treated at an early stage of the disease.