Postmortem diagnosis of Diamond-Blackfan anemia |
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Authors: | Beauchamp-Nicoud Anne Da Costa Lydie Proust Alexis Rincé Patricia Saker Safa Tchernia Gil |
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Affiliation: | CHU Kremlin-Bicêtre, Laboratoire d'Hématologie, Hopital Bicêtre, 78 rue Général Leclerc, 92375 Le Kremlin-Bicêtre, France. anne.beauchamp_nicoud@caramail.com |
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Abstract: | 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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