Glycogen storage disease type II (Pompe disease) in children

The paper gives the data available in the literature, which reflect the manifestations, diagnosis, and current treatments of the rare (orphan) inherited disease glycogen storage disease type II or Pomp disease in children, as well as its classification. The infant form is shown to be most severe, re...

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Bibliographic Details
Main Authors: A. N. Semyachkina, V. S. Sukhorukov, T. M. Bukina, M. I. Yablonskaya, E. S. Merkuryeva, M. N. Kharabadze, E. A. Proskurina, E. Yu. Zakharova, A. V. Brydun, P. A. Shatalov, P. V. Novikov
Format: Article
Language:Russian
Published: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Series:Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:
Online Access:https://www.ped-perinatology.ru/jour/article/view/58