Clinical study of respiratory function in patients with late-onset glycogen storage disease typeⅡ

Clinical study of respiratory function in patients with late-onset glycogen storage disease typeⅡ

<p><strong>Background</strong> Late-onset glycogen storage disease typeⅡ(GSDⅡ, Pompe disease) is an autosomal recessive disease exhibiting progressive proximal skeletal muscle weakness and respiratory muscle involvement, caused by deficiency of the lysosomal enzyme acid α-glucos...

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Bibliographic Details
Main Authors: Wei-na JIN, Cheng-li QUE, Hai-yan TANG, Yu HUANG, Zhao-xia WANG, Xiao LIU, He LÜ, Wei ZHANG, Yun YUAN
Format: Article
Language:English
Published: Tianjin Huanhu Hospital 2014-05-01
Series:Chinese Journal of Contemporary Neurology and Neurosurgery
Subjects:
Glycogen storage disease typeⅡ
Alpha-glucosidases
Respiratory function tests
Online Access:http://www.cjcnn.org/index.php/cjcnn/article/view/951

Internet

http://www.cjcnn.org/index.php/cjcnn/article/view/951

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