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Infantile Pompe disease: A case report and review of the Chinese literature
Pompe disease, also known as glycogen storage disease type II, is caused by acid maltase deficiency, and can lead to lysosomal glycogen storage. The primal manifestations may be observed in children and adults, and also in infants. In general, the clinical spectrum in infants is more progressive and...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4726885/ https://ncbi.nlm.nih.gov/pubmed/26889246 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2015.2862 |
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