Literature DB >> 11774119

A patient with adult-onset type II citrullinemia on long-term hemodialysis: reversal of clinical symptoms and brain MRI findings.

Saori Oshiro1, Tutomu Kochinda, Takeshi Tana, Masanobu Yamazato, Keiko Kobayashi, Yukihiro Komine, Hiromi Muratani, Takeyori Saheki, Kunitoshi Iseki, Shuichi Takishita.   

Abstract

A 40-year-old woman was referred for several episodes of coma lasting from 2 hours to 2 days. She had been on maintenance hemodialysis for polycystic kidney disease for 9 months. Laboratory findings showed high serum levels of ammonia and citrulline, and a diagnosis of adult-onset type II citrullinemia was made. Multiple areas of focal brain edema were shown by magnetic resonance imaging. The clinical manifestations of coma and abnormal behavior were resolved with intensified dialysis (ie, four 5-hour sessions per week with glycerol and continuous ambulatory peritoneal dialysis). No abnormal shadow was present on follow-up magnetic resonance imaging. Such intensified dialysis therapy may be effective for adult-onset type II citrullinemia and may be applicable even in patients who do not have end-stage renal disease if liver transplant is not an option. Copyright 2002 by the National Kidney Foundation, Inc.

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Year:  2002        PMID: 11774119     DOI: 10.1053/ajkd.2002.29915

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  3 in total

Review 1.  In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.

Authors:  Erica B Sherry; Phil Lee; In-Young Choi
Journal:  Neurochem Res       Date:  2015-11-26       Impact factor: 3.996

2.  Neonatal citrullinemia: comparison of conventional MR, diffusion-weighted, and diffusion tensor findings.

Authors:  Charles B L M Majoie; Jeroen M Mourmans; Erik M Akkerman; Marinus Duran; Bwee Tien Poll-The
Journal:  AJNR Am J Neuroradiol       Date:  2004-01       Impact factor: 3.825

3.  Identification of 13 novel mutations including a retrotransposal insertion in SLC25A13 gene and frequency of 30 mutations found in patients with citrin deficiency.

Authors:  Ayako Tabata; Jian-Sheng Sheng; Miharu Ushikai; Yuan-Zong Song; Hong-Zhi Gao; Yao-Bang Lu; Fumihiko Okumura; Mikio Iijima; Kozo Mutoh; Shosei Kishida; Takeyori Saheki; Keiko Kobayashi
Journal:  J Hum Genet       Date:  2008-04-05       Impact factor: 3.172

  3 in total

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