Clinical diagnosis and treatment of three cases with hyperornithinemia-hyperammonemia-homocitrullinuria syndrome

Objective: To study the clinical characteristics, methods of diagnosis and treatment of hyperornithinemia-hyperammonemia- homocitrullinuria (HHH) syndrome. Method: From July 2011 to August 2016, 3 Chinese patients with HHH syndrome were enrolled in this study. The clinical course, biochemical featur...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 55(2017), 6 vom: 02. Juni, Seite 428-433
1. Verfasser:	Guan, H Z (VerfasserIn)
Weitere Verfasser:	Ding, Y, Li, D X, Dong, H, Song, J Q, Jin, Y, Zhu, Z J, Sun, L Y, Yang, Y L
Format:	Online-Aufsatz
Sprache:	Chinese
Veröffentlicht:	2017
Zugriff auf das übergeordnete Werk:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:	Journal Article HHH syndrome Ornithine transporter SLC25A15 Urea cycle disorder, inborn Proteins Orotic Acid 61H4T033E5 Arginine 94ZLA3W45F mehr... Ornithine E524N2IXA3 Carnitine S7UI8SM58A