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Urines of 11 patients with three different types of mucolipidosis characterized by a total or partial sialidase deficiency, were studied. In all cases, we found an important accumulation of sialyl-oligosaccharides. The structure of 9 of them has been determined: α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)-β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)-β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[α-Man-(16)]β-Man-(14)-GlcNAc, α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[β-Gal-(14)-β-GlcNAc-(12)-α-Man-(16)]β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[β-Gal-(14)-β-GlcNAc-(12)-α-Man-(16)]β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)[α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(14)]α-Man-(13)-β-Man-(14)-GlcNAc, α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(16)]β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[α-AcNeu-(23)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(16)]β-Man-(14)-GlcNAc, α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(13)[α-AcNeu-(26)-β-Gal-(14)-β-GlcNAc-(12)-α-Man-(16)]β-Man-(14)-GlcNAc. All these compounds are products of incomplete catabolism of glycoproteins and result from the action of a new type of β-endo-N-acetylglucosaminidase able to act on sialylated glycoproteins or glycopeptides. The term sialidosis is proposed for these three types of oligosaccharidosis.
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Strecker et al. (1977) studied this question.
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