原发性和后天性难治性铁粒幼细胞贫血（作者译）
[Refractory sideroblastic anaemia of primary and acquired appearance (author's transl)].
作者信息
Albahary C, Boiron M, Najean Y
出版信息
Nouv Presse Med. 1979 Feb 3;8(6):425-6.
PMID:162300
Abstract
This anaemia begun at the age of 40 years. The patient died 17 years later. There was no leukaemic transformation. The authors describe the enzyme abnormalities found in the red cells (increased urosynthetase) and/for of raised serum iron levels in relatives, such that the truly acquired and apparently primary nature of this blood disease must be brought into question.
摘要
这种贫血始于40岁。患者17年后死亡。未发生白血病转化。作者描述了在红细胞中发现的酶异常（尿卟啉原合成酶增加）以及亲属血清铁水平升高的情况，因此这种血液疾病真正后天获得性及明显原发性的性质必须受到质疑。
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