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2.
Rev Esp Enferm Dig ; 111(2): 168-169, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30318896

ABSTRACT

Type III glycogen storage disease (GSD-III) is an autosomal recessive disorder due to the deficiency of the glycogen debrancher enzyme. 80% of the patients have hepatic and muscular involvement (IIIa), compared to 15% with only liver involvement (IIIb). As the life expectancy improves in these patients, the possible liver complications are better understood.


Subject(s)
Carcinoma, Hepatocellular/surgery , Glycogen Storage Disease Type III/surgery , Liver Cirrhosis/surgery , Liver Neoplasms/surgery , Liver Transplantation , Adult , Glycogen Storage Disease Type III/complications , Humans , Male , Middle Aged , Neoplasm Recurrence, Local
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