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медицина
мукополисахаридоз V типа
синдром Шейе
медицина
мукополисахаридоз
медицина
дистрофическая дисплазия
мукополисахаридоз VI типа
синдром Марото-Лами
Sly syndrome, also called mucopolysaccharidosis type VII (MPS-VII), is an autosomal recessive lysosomal storage disease caused by a deficiency of the enzyme β-glucuronidase. This enzyme is responsible for breaking down large sugar molecules called glycosaminoglycans (AKA GAGs, or mucopolysaccharides). The inability to break down GAGs leads to a buildup in many tissues and organs of the body. The severity of the disease can vary widely.