Goebel H H, Ikeda K, Schulz F, Burck U, Kohlschütter A
Acta Neuropathol. 1981;55(3):247-9. doi: 10.1007/BF00691325.
Fingerprint (FP) profiles in vacuolated lymphocytes of mucopolysaccharidoses I-H, II, III-A, and III-B are a numerically rare, but possibly consistent finding as they have not been seen in vacuolated lymphocytes of other non-neuronal lipofuscinosis (NCL) lysosomal diseases. Their nosologic significance is not clear, but they may be as non-specific as tubular inclusions in lymphocytes and they are identical to those FP profiles seen in juvenile NCL.
黏多糖贮积症I-H型、II型、III-A型和III-B型空泡淋巴细胞中的指纹(FP)图谱数量上较为罕见,但可能是一致的发现,因为在其他非神经元性脂褐质沉积症(NCL)溶酶体疾病的空泡淋巴细胞中未见到。它们的疾病分类学意义尚不清楚,但可能与淋巴细胞中的管状包涵体一样不具有特异性,并且与青少年NCL中所见的FP图谱相同。