Liver cirrhosis treated by living donor liver transplantation in a patient with AGL mutation c.2607-2610delATTC and c.1672dupA.

Kondo, Yuichi; Usui, Hiromi; Ishige-Wada, Mika; Murase, Toshio; Owada, Misao; Okubo, Minoru

Kondo, Yuichi; Usui, Hiromi; Ishige-Wada, Mika; Murase, Toshio; Owada, Misao; Okubo, Minoru.

Affiliation

Kondo Y; Okinaka Memorial Institute for Medical Research, Tokyo, Japan.

Clin Chim Acta ; 424: 19-21, 2013 Sep 23.

Article in En | MEDLINE | ID: mdl-23688858

Subject(s)

Glycogen Storage Disease Type III/therapy; Liver Cirrhosis/therapy; Liver Transplantation; Mutation; alpha-Glucosidases/genetics; Glycogen Storage Disease Type III/complications; Glycogen Storage Disease Type III/diagnosis; Glycogen Storage Disease Type III/genetics; Heterozygote; Humans; Liver Cirrhosis/complications; Liver Cirrhosis/diagnosis; Liver Cirrhosis/genetics; Living Donors; Male; Treatment Outcome; Young Adult; alpha-Glucosidases/deficiency

Key words

AGL; Glycogen storage disease type III; Liver cirrhosis; Living donor liver transplantation; Mutation

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Glycogen Storage Disease Type III / Liver Transplantation / Alpha-Glucosidases / Liver Cirrhosis / Mutation Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: Clin Chim Acta Year: 2013 Document type: Article Affiliation country: Japan Country of publication: Netherlands

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