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Swallow Prognosis and Follow-Up Protocol in Infantile Onset Pompe Disease
Oro-pharyngeal dysphagia commonly occurs in patients with infantile onset Pompe disease (IOPD), which is a rare recessive neuromuscular disorder caused by deficiency of the lysosomal enzyme acid alpha-glucosidase. Without treatment, death occurs by 1 year of age from cardiorespiratory failure. Enzym...
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| Yayımlandı: | JIMD Rep |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Springer Berlin Heidelberg
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5413449/ https://ncbi.nlm.nih.gov/pubmed/27344650 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2016_576 |
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