【用戶】PPMTPASS
【年級】國三上
【評論內容】People with Gaucher disease lack the normal form of the glucocerebrosidase enzyme and are unable to break down glucocerebroside. Instead, the glucocerebroside remains stored within the lysosomes, preventing the macrophages from functioning normally. Enlarged macrophages containing undigested glucocerebroside are called Gaucher cells. These cells are the hallmark of this disease.
【用戶】陳育惠
【年級】高三上
【評論內容】高歇氏病（Gaucher氏症）又叫白塞氏綜合徵或眼，口，生殖器綜合徵，或，即家族性脾性貧血症。是先天葡萄糖腦苷酯酶缺乏引起的罕見的代謝遺傳病，主要侵犯肝，脾，淋巴結，肺及骨髓等單核巨噬細胞系統。缺乏這種酶，會導致葡萄糖腦苷酯在巨噬細胞內堆積而成為高歇氏細胞