Hamel B C, Schretlen E D
Eur J Pediatr. 1982 Mar;138(2):130-5. doi: 10.1007/BF00441138.
Sideroblastic Anaemias are characterised by a) chronic hypochromic anemia, b) ringed sideroblasts in the bone marrow, c) an increase in total body iron, d) ineffective erythropoiesis and e) often abnormal concentrations of F.E.P. A classification of Sideroblastic Anaemia is given and the pathophysiology of Sideroblastic Anaemia is discussed. A series of seven paediatric cases with Sideroblastic Anaemia is presented and the results of studies of the iron, vitamin B6 and porphyrin metabolism are discussed. In two cases arguments for an ALA-synthetase deficiency are given. All five males were diagnosed as hereditary X-linked Sideroblastic Anaemia, one female as I.R.S.A. and the other female, who showed the features of the X-linked type, as congenital Sideroblastic Anaemia.
a) 慢性低色素性贫血,b) 骨髓中出现环形铁粒幼细胞,c) 全身铁含量增加,d) 无效红细胞生成,以及e) 血清铁蛋白浓度常异常。本文给出了铁粒幼细胞性贫血的分类,并讨论了其病理生理学。本文报告了7例小儿铁粒幼细胞性贫血病例,并讨论了铁、维生素B6和卟啉代谢的研究结果。在2例病例中给出了支持δ-氨基-γ-酮戊酸合成酶缺乏的论据。所有5名男性被诊断为遗传性X连锁铁粒幼细胞性贫血,1名女性为特发性获得性铁粒幼细胞性贫血,另1名表现出X连锁型特征的女性为先天性铁粒幼细胞性贫血。