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Autor:
Nato D. Vashakmadze, Natalya V. Zhurkova, Olga B. Gordeeva, Elena V. Komarova, Tatyana E. Privalova, Anastasya I. Rykunova, Marina А. Babaykina
Publikováno v:
Вопросы современной педиатрии, Vol 20, Iss 6s, Pp 618-623 (2021)
Mucopolysaccharidosis type II (MPS II; Hunter syndrome) is X-linked hereditary disease from the group of lysosomal storage disease. Its prevalence is 3–7 cases per 1 million live-born boys. MPS II occurs due to the deficiency of iduronate-2-sulfata
Externí odkaz:
https://doaj.org/article/8bcea21d0889433c97c852e58a4410f7
