Postmortem diagnosis of Diamond-Blackfan anemia

被引:0
作者
Beauchamp-Nicoud, A
Da Costa, L
Proust, A
Rincé, P
Saker, S
Tchernia, G
机构
[1] CHU Kremlin Bicetre, Hematol Lab, Assistance Publ Hop Paris, Fac Med Paris 11, Le Kremlin Bicetre, France
[2] Genethon, Ctr Res & Applicat Gene Therapies, Evry, France
关键词
neonatal anemia; Diamond-Blackfan anemia; pure red cell aplasia; RPS19; gene; blood filter paper;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diamond-Blackfan anemia (DBA) is a rare etiology for congenital anemia, but this diagnosis should be considered when aregenerative hypoplastic anemia occurs in infancy. A term infant girl received a red blood cell transfusion at birth for neonatal anemia (hemoglobin 75 g/L) initially attributed to abruptio placentae. There were no additional investigations. Hemoglobin gradually decreased during the first 4 weeks of life, leading to severe anemia and death despite transfusions. A postmortem diagnosis of DBA was made by extraction of DNA collected on blood filter paper showing a deletion in RPS19 gene. Neonatal anemias should be carefully investigated and close follow-up should be performed during the first months of life, even if there is an obvious hemorrhagic etiology.
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页码:847 / 848
页数:2
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