Two cases of a non-progressive hepatic form of glycogen storage disease type IV with atypical liver pathology

Glycogen storage disease type IV (GSD IV) is a rare inborn metabolic disorder characterized by the accumulation of amylopectin-like glycogen in the liver or other organs. The hepatic subtype may appear normal at birth but rapidly develops to liver cirrhosis in infancy. Liver pathological findings he...

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Detalles Bibliográficos
Autores principales: Ichimoto, Keiko, Fujisawa, Tomoo, Shimura, Masaru, Fushimi, Takuya, Tajika, Makiko, Matsunaga, Ayako, Ogawa-Tominaga, Minako, Akiyama, Nana, Naruke, Yuki, Horie, Hiroshi, Fukuda, Tokiko, Sugie, Hideo, Inui, Ayano, Murayama, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235638/
https://www.ncbi.nlm.nih.gov/pubmed/32455116
http://dx.doi.org/10.1016/j.ymgmr.2020.100601

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235638/
https://www.ncbi.nlm.nih.gov/pubmed/32455116
http://dx.doi.org/10.1016/j.ymgmr.2020.100601

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