Open AccessLysosomal storage diseases. Mucopolysaccharidosis types IV, VI, and VII – Morquio, Maroto–Lamy and Sly syndrome
Author(s) -
V. N. Gorbunova,
Natalia V. Buchinskaia
Publication year - 2022
Publication title -
pediatrician (st petersburg)
Language(s) - English
Resource type - Journals
eISSN - 2587-6252
pISSN - 2079-7850
DOI - 10.17816/ped126107-125
Subject(s) - hurler syndrome , mucopolysaccharidosis , substrate reduction therapy , lysosomal storage disease , sulfatase , gangliosidosis , medicine , dermatan sulfate , pathogenesis , keratan sulfate , hypophosphatasia , enzyme replacement therapy , glucocerebrosidase , immunology , chondroitin sulfate , disease , biology , pathology , glycosaminoglycan , biochemistry , enzyme , anatomy , alkaline phosphatase
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