THE USE OF LYSINE SUPPLEMENTATION IN A CHILD WITH ORNITHINE δ-AMINOTRANSFERASE DEFICIENCY

被引:0
|
作者
MacDonald, A. [1 ]
Fullerton, D. [1 ]
Preece, M. A. [1 ]
Daly, A. [1 ]
Gokmen-Ozel, H. [1 ]
Neville, C. [1 ]
Vijay, S. [1 ]
Santra, S. [1 ]
Hendriksz, C. [1 ]
Chakrapani, A. [1 ]
机构
[1] Childrens Hosp, Birmingham B16 8ET, W Midlands, England
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
723
引用
收藏
页码:146 / 146
页数:1
相关论文
共 50 条
  • [31] Protracted Cortical Visual Loss in a Child With Ornithine Transcarbamylase Deficiency
    Anderson, Jennifer M.
    Brodsky, Michael C.
    JOURNAL OF NEURO-OPHTHALMOLOGY, 2010, 30 (01) : 99 - 102
  • [32] Considerations on urea cycle disorders: a child with ornithine transcarbamylase deficiency
    Bellido, M.
    Gonzalez Perez, M.
    Martinez Ruiz, A.
    Barcelo, I.
    PEDIATRIC ANESTHESIA AND CRITICAL CARE JOURNAL, 2016, 4 (01): : 28 - 29
  • [33] A novel mutation in ornithine transcarbamylase gene identified from a Chinese child with ornithine transcarbamylase deficiency
    Wu, Bo
    Wang, Yi-Zheng
    Cao, Li-Rong
    Zhang, Rui-Ping
    Fang, Yu-Lian
    Zhang, Yu-Qin
    Cai, Chun-Quan
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2018, 11 (06): : 6344 - 6350
  • [34] ORNITHINE AMINOTRANSFERASE ACTIVITY, TISSUE ORNITHINE CONCENTRATIONS AND POLYAMINE METABOLISM
    SEILER, N
    DAUNE, G
    BOLKENIUS, FN
    KNODGEN, B
    INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1989, 21 (04): : 425 - 432
  • [35] ACTIVITIES OF ORNITHINE AMINOTRANSFERASE AND ORNITHINE DECARBOXYLASE IN CHRONICALLY UREMIC RATS
    WANG, M
    SCHUTZ, I
    KOPPLE, J
    SWENDSEID, M
    LIFE SCIENCES, 1981, 28 (21) : 2349 - 2354
  • [36] Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation
    Tanyel Zubarioglu
    Ertugrul Kiykim
    Mehmet Serif Cansever
    Cigdem Aktuglu Zeybek
    The Indian Journal of Pediatrics, 2016, 83 : 754 - 755
  • [37] Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation
    Zubarioglu, Tanyel
    Kiykim, Ertugrul
    Cansever, Mehmet Serif
    Zeybek, Cigdem Aktuglu
    INDIAN JOURNAL OF PEDIATRICS, 2016, 83 (07): : 754 - 755
  • [38] A neonate with ornithine aminotransferase deficiency; insights on the hyperammonemia-associated biochemical phenotype of gyrate atrophy
    Kaczmarczyk, Aneta
    Baker, Mark
    Diddle, Julianna
    Yuzyuk, Tatiana
    Valle, David
    Lindstrom, Kristin
    MOLECULAR GENETICS AND METABOLISM REPORTS, 2022, 31
  • [39] ORNITHINE AMINOTRANSFERASE IN HUNTINGTONS-DISEASE
    WONG, PTH
    MCGEER, PL
    ROSSOR, M
    MCGEER, EG
    BRAIN RESEARCH, 1982, 231 (02) : 466 - 471
  • [40] Ornithine aminotransferase as a therapeutic target in hyperammonemias
    Seiler, N
    ADVANCES IN CIRRHOSIS, HYPERAMMONEMIA, AND HEPATIC ENCEPHALOPATHY, 1997, 420 : 113 - 142