Management and outcome of neonatal-onset ornithine transcarbamylase deficiency following liver transplantation at 60 days of life

被引:21
作者
Ensenauer, R
Tuchman, M
El-Youssef, M
Kotagal, S
Ishitani, MB
Matern, D
Babovic-Vuksanovic, D
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Dept Med Genet, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Coll Med, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Coll Med, Dept Pediat & Adolescent Med, Rochester, MN 55905 USA
[4] Mayo Clin & Mayo Fdn, Coll Med, Div Child Neurol, Rochester, MN 55905 USA
[5] Mayo Clin & Mayo Fdn, Coll Med, Dept Surg, Rochester, MN 55905 USA
[6] George Washington Univ, Childrens Natl Med Ctr, Washington, DC USA
关键词
ornithine transcarbamylase deficiency; ornithine carbarnoyltransferase deficiency; hyperammonemia; infantile liver transplantation; citrulline supplementation;
D O I
10.1016/j.ymgme.2004.12.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Neonatal hyperammonemia secondary to X-linked ornithine transcarbamylase (OTC) deficiency carries a high risk of morbidity and mortality. Results of medical therapy are less than satisfactory. Experience with liver transplantation in very young affected infants is limited. We report a male newborn with severe OTC deficiency who underwent successful orthotopic, cadaveric liver transplantation at the age of 60 days. Although technically challenging in the neonatal period, liver transplantation should be considered early as the most promising treatment approach currently available. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:363 / 366
页数:4
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