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Alpha-mannosidosis in children: analysis of the observations and treatment options

The article is devoted to a rare (orphan) disease from the group of lysosomal storage diseases — alpha-mannosidosis, associated with the accumulation of mannose-containing oligosaccharides in the tissues and cells of the body. The authors analyze the literature data and proposals of the Internationa...

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Main Authors: A. N. Semyachkina, E. A. Nikolaeva, E. Yu. Voskoboeva, M. A. Dantseva, E. Yu. Zakharova
Formato: Artigo
Idioma:Russo
Publicado em: Ltd. “The National Academy of Pediatric Science and Innovation” 2020-09-01
Colecção:Rossijskij Vestnik Perinatologii i Pediatrii
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Acesso em linha:https://www.ped-perinatology.ru/jour/article/view/1213
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