Você procurou por: glucocerebroside (Maltês - Inglês)

nies bil- marda ma jkollhomx biżżejjed minn enzim, imsejjaħ glucocerebroside.
people with the disease do not have enough of an enzyme, glucocerebrosidase.

dan l- enzim normalment ikisser il- prodott skartat xaħmi imsejjaħ glucocerebroside.
this enzyme normally breaks down a fatty waste product called glucocerebroside.

l-akkumulazzjoni ta’ glucocerebroside fil-fwied u l-milsa twassal għal organomegalija.
the accumulation of glucocerebroside in the liver and spleen leads to organomegaly.

imiglucerase tgħin fit- tkissir (tikkatalizza) ta ’ glucocerebroside u twaqqaf il- bini tiegħu fil- ġisem.
imiglucerase helps (catalyses) the break down of glucocerebroside and stops it building up in the body.

il-marda gaucher hija disturb rari li jintiret, li fiha persuna ma jkollhiex biżżejjed mill-enzima msejħa glucocerebrosidase, li normalment tkisser xaħam imsejjaħ glucocerebroside.
gaucher disease is a rare inherited disorder, in which people do not have enough of an enzyme called glucocerebrosidase, which normally breaks down a fat called glucocerebroside.

dan in-nuqqas ta’ enzimi jikkawża akkumulazzjoni ta’ glucocerebroside l-aktar f’makrofaġi, li joħloq ċelloli fowm jew “ċelloli gaucher”.
this enzymatic deficiency causes an accumulation of glucocerebroside primarily in macrophages, giving rise to foam cells or "gaucher cells".