Kuribayashi T, Uchida S, Kuroume T, Umegae S, Omine M, Maekawa T
Blut. 1979 Sep;39(3):201-9. doi: 10.1007/BF01008449.
This is the first case of two siblings with congenital dyserythrobpoietic anemia (CDA) type I to be reported from a Japanese family. Both of these cases showed characteristic morphological aberration of erythroid precursors, ineffective erythropoiesis, and negative acidified serum test. The ultrastructural study of erythroblasts also revealed characteristics quite compatible with CDA type I.
这是首例报道的来自一个日本家庭的两例患有I型先天性红细胞生成异常性贫血(CDA)的兄弟姐妹。这两例患者均表现出红系前体细胞的特征性形态异常、无效红细胞生成以及酸化血清试验阴性。对成红细胞的超微结构研究也揭示了与I型CDA完全相符的特征。