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Liver Transplantation for Glycogen Storage Disease Type IV
Glycogen storage disease type IV (GSD IV) is a rare autosomal recessive disorder caused by glycogen–branching enzyme (GBE) deficiency, leading to accumulation of amylopectin–like glycogen that may damage affected tissues. The clinical manifestations of GSD IV are heterogeneous; one of which is the c...
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| Udgivet i: | Front Pediatr |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Frontiers Media S.A.
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7933444/ https://ncbi.nlm.nih.gov/pubmed/33681109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2021.633822 |
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