Late-onset Pompe disease with complicated intracranial aneurysm: a Chinese case report

Pompe disease is a rare autosomal recessive hereditary disease caused by genetic defects of acid maltase. This disease could be divided into two forms: infantile and late-onset, which mainly affect cardiac, respiratory, and skeletal muscle systems. Late-onset patients mainly show symptoms of skeleta...

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Detalles Bibliográficos
Autores principales: Zhang, Bin, Zhao, Yuying, Liu, Junling, Li, Ling, Shan, Jingli, Zhao, Dandan, Yan, Chuanzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820213/
https://www.ncbi.nlm.nih.gov/pubmed/27099502
http://dx.doi.org/10.2147/NDT.S94892

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820213/
https://www.ncbi.nlm.nih.gov/pubmed/27099502
http://dx.doi.org/10.2147/NDT.S94892

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