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Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia.

Sevil DorumCengiz Havalı
Published 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.
Keyphrases
  • early stage
  • case report
  • copy number
  • genome wide
  • squamous cell carcinoma
  • replacement therapy
  • genome wide analysis