McMahon J N, Lieberman J E, Gordon-Smith E C, Egan E L
Clin Lab Haematol. 1981;3(1):27-34. doi: 10.1111/j.1365-2257.1981.tb01306.x.
Hereditary haemolytic anaemia with basophilic stippling caused by pyrimidine 5'-nucleotidase deficiency is described in three members of two unrelated Irish families. In one family, the disease was moderately severe and the patient's condition was improved by splenectomy. In the other family the haemolytic anaemia was well compensated. In neither family was there a marked elevation of reduced glutathione. The implications are that pyrimidine 5'-nucleotidase deficiency is a heterogeneous disorder, both clinically and biochemically. In more severe forms splenectomy may be beneficial.
两个不相关的爱尔兰家庭的三名成员患有由嘧啶5'-核苷酸酶缺乏引起的遗传性溶血性贫血伴嗜碱性点彩红细胞。在一个家庭中,病情中度严重,脾切除术后患者状况有所改善。在另一个家庭中,溶血性贫血得到了很好的代偿。两个家庭中还原型谷胱甘肽均未显著升高。这意味着嘧啶5'-核苷酸酶缺乏在临床和生化方面都是一种异质性疾病。在更严重的形式中,脾切除术可能有益。