| Literature DB >> 12132524 |
Yasuhiro Takashima1, Makoto Koide, Hideyuki Fukunaga, Masahide Iwai, Masaki Miura, Ryoji Yoneda, Tsuneo Fukuda, Keiko Kobayashi, Takeyori Saheki.
Abstract
A 21-year-old woman was admitted with altered consciousness and hyperammonemia. She was diagnosed as having adult-onset type II citrullinemia (CTLN2) by DNA analysis. The patient had mutations of the SLC25A13 gene, which were compound heterozygotes of 851 del 4 and IVS11+1G>A. CTLN2 has a poor prognosis, in spite of various intensive medications, and we performed a living related partial liver transplantation (LRLT). Over a 2-year follow-up, the patient has been well. CTLN2 can be diagnosed by the DNA analysis and can be treated by LRLT.Entities:
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Year: 2002 PMID: 12132524 DOI: 10.2169/internalmedicine.41.555
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271