Fatigue and quality of life in citrin deficiency during adaptation and compensation stage

Citrin-deficient children and adolescents between adult-onset type II citrullinemia and neonatal intrahepatic cholestasis by citrin deficiency do not have clear clinical features except for unusual diet of high-fat, high-protein, and low-carbohydrate food. The aims of the present study are to charac...

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Veröffentlicht in:Molecular genetics and metabolism 2013-05, Vol.109 (1), p.9-13
Hauptverfasser: Okano, Yoshiyuki, Kobayashi, Kyoko, Ihara, Kenji, Ito, Tetsuya, Yoshino, Makoto, Watanabe, Yoriko, Kaji, Shunsaku, Ohura, Toshihiro, Nagao, Masayoshi, Noguchi, Atsuko, Mushiake, Sotaro, Hohashi, Naohiro, Hashimoto-Tamaoki, Tomoko
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Sprache:eng
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Zusammenfassung:Citrin-deficient children and adolescents between adult-onset type II citrullinemia and neonatal intrahepatic cholestasis by citrin deficiency do not have clear clinical features except for unusual diet of high-fat, high-protein, and low-carbohydrate food. The aims of the present study are to characterize fatigue and quality of life (QOL) in citrin-deficient patients during adaptation and compensation stage, and to define the relationship between fatigue and QOL. The study subjects were 55 citrin-deficient patients aged 1–22years (29 males) and 54 guardians. Fatigue was evaluated by self-reports and proxy-reports of the PedsQL Multidimensional Fatigue Scale. QOL was evaluated by the PedsQL Generic Core Scales. Both scale scores were significantly lower in child self-reports (p
ISSN:1096-7192
1096-7206
DOI:10.1016/j.ymgme.2013.01.020