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polyneuropathy organomegalies
poems-syndrom
Last Update: 2014-12-09
Usage Frequency: 1
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organomegalies, polyneuropathy
poems-syndrom
Last Update: 2014-12-09
Usage Frequency: 1
Quality:
due to the missing or defective iduronate-2-sulfatase enzyme in patients with hunter syndrome, glycosaminoglycans progressively accumulate in the cells, leading to cellular engorgement, organomegaly, tissue destruction, and organ system dysfunction.
beroende på avsaknad av eller brist på iduronat-2-sulfatasenzym hos patienter med hunters syndrom, ackumuleras successivt glykosaminoglykaner i cellerna, vilket leder till cellulär blodöverfyllnad, organomegali, vävnadsförstörelse och organsystemsdysfunktion.
Last Update: 2017-04-26
Usage Frequency: 3
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