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mukopolisacharidozės
diagnosis of mucopolysaccharidosis
Last Update: 2013-12-21
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Šis vaistas gali palengvinti vi tipo mukopolisacharidozės simptomus.
this medicine may improve the symptoms of mps vi.
Last Update: 2017-04-26
Usage Frequency: 1
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jie susikaupia daugelyje kūno audinių, sukeldami vi tipo mukopolisacharidozės simptomus.
they accumulate in many tissues in the body, which causes the symptoms of mps vi.
Last Update: 2017-04-26
Usage Frequency: 1
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hunterio sindromas, dar žinomas ii tipo mukopolisacharidozės pavadinimu, yra reta paveldima liga, kuria daugiausia serga vyrai.
hunter syndrome, which is also known as mucopolysaccharidosis ii, is a rare, inherited disease that primarily affects male patients.
Last Update: 2017-04-26
Usage Frequency: 1
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hunter’ io sindromas, kuris dar žinomas ii tipo mukopolisacharidozės pavadinimu, yra paveldima liga, kuria daugiausia serga vyrai.
hunter syndrome, which is also known as mucopolysaccharidosis ii, is a rare, inherited disease that primarily affects male patients.
Last Update: 2012-04-11
Usage Frequency: 2
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mukopolisacharidozės – tai kaupimosi lizosomose sutrikimai, kuriuos sukelia tam tikrų lizosomų fermentų, reikalingų glikozaminoglikanų (gag) katabolizmui, trūkumas.
mucopolysaccharidoses comprises a group of lysosomal storage disorders caused by the deficiency of specific lysosomal enzymes required for the catabolism of glycosaminoglycans (gag).
Last Update: 2017-04-26
Usage Frequency: 1
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aldurazyme yra skirtas pacientų, kurie serga mps i (mukopolisacharidozė i) liga, gydymui.
aldurazyme is used to treat patients with mps i disease (mucopolysaccharidosis i).
Last Update: 2017-04-26
Usage Frequency: 3
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