Infantile Pompe disease: Clinical picture, diagnosis, and treatment

Pompe disease is a rare inherited disease that belongs to lysosomal accumulation diseases and can be considered as cardiac glycogenosistype II, as well as a severe neuromuscular disease or metabolic myopathy. Physicians of different specialties very rarely identify this pathology, which is due to bo...

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Bibliographic Details
Main Authors: N. P. Kotlukova, S. V. Mikhailova, T. M. Bukina, E. Yu. Zakharova
Format: Article
Language:Russian
Published: ABV-press 2015-02-01
Series:Нервно-мышечные болезни
Subjects:
Online Access:https://nmb.abvpress.ru/jour/article/view/101