| Literature DB >> 26190618 |
Akira Ueda1,2, Kazuhiko Okada2, Terumi Takahara3, Keiichi Iwasa2, Kazuko Shinagawa2, Akio Entani2, Syuji Inatsuchi2, Takayuki Ando1, Haruka Fujinami1, Kazuto Tajiri1, Yoshiharu Tokimitsu1, Kohei Ogawa1, Takayoshi Miyazono1, Takako Miyazaki1, Jun Murakami1, Ayumu Hosokawa1, Satoshi Yasumura1, Masami Minemura1, Takahiko Kudo1, Toshiro Sugiyama1.
Abstract
A 47-year-old Japanese man was first admitted to our hospital for 8 days because of an asthma attack. After discharge he changed his diet. On the 12th day after his discharge, he was re-admitted to our hospital because he exhibited transient loss of consciousness with flapping tremor. His plasma ammonia level was extremely high (245 μg/dL; normal, <90 μg/dL), suggesting hepatic encephalopathy. He underwent intravenous administration of branched-chain amino acids (Aminoleban(®)) and oral administration of lactulose and kanamycin sulfate; however, the hyperammonemia did not improve. Analysis of the amino acids and citrin gene led to the diagnosis of adult-onset type II citrullinemia (CTLN2). Following this diagnosis, the carbohydrate content of his diet was mildly restricted. As a result, his plasma ammonia level markedly improved (ammonia, 40-60 μg/dL) and he became symptom-free without any medication. CTLN2 is a metabolic disorder characterized by increased plasma concentrations of citrulline and ammonia, which occurs by the failure of compensatory mechanisms associated with diet. Here, we report a case of a patient for whom a change in eating habits during his hospitalization disturbed his compensatory mechanism resulting in clinical CTLN2, which was reversed with an appropriate diet.Entities:
Keywords: CTLN2; Citrin; Citrullinemia; Hepatic encephalopathy; Hyperammonemia; SLC25A13
Year: 2010 PMID: 26190618 DOI: 10.1007/s12328-010-0188-3
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265