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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: A new UHPLC-MS/MS method for the screening of urinary oligosaccharides expands the detection of storage disorders

Fig. 3

Scatter charts of disorders presenting an increased excretion of Glc4 which included, besides Pompe disease, also the autophagy related disorders Vici and Yunis-Varon syndromes, and Danon disease. The figure shows the scatter charts in urine (top panel) and DUS (lower panel) of the transition 665 > 179 of the tetrasaccharide 6-α-D-glucopyranosyl-maltotriose (Glc4) in Pompe disease, Vici syndrome, Yunis-Varon syndrome, and Danon disease in comparison to controls

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172