Primary Hyperoxaluria in Korean Pediatric Patients

• Autores principales: Yunsoo Choe (Autor), Jiwon M. Lee (Autor), Ji Hyun Kim (Autor), Myung Hyun Cho (Autor), Seong Heon Kim (Autor), Joo Hoon Lee (Autor), Young Seo Park (Autor), Hee Gyung Kang (Autor), Il Soo Ha (Autor), Hae Il Cheong (Autor)
• Formato: Libro
• Publicado: Korean Society of Pediatric Nephrology, 2019-10-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

Background Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 1-3 (PH1-PH3) caused by AGXT, GRHPR, and HOGA1 gene mutations, respectively. We performed a retrospective case series study of Kore...