1.
Clin Case Rep
; 3(6): 392-5, 2015 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26185635
RESUMO
Diamond-Blackfan anemia (DBA) is a congenital erythroid aplasia usually diagnosed in the early infancy and associated with mutations or large deletions in 11 ribosomal protein (RP) genes. Adult patients with severe, transfusion dependence, aregenerative anemia might have a genetic-in-origin disease with an atypical presentation. Late onset nonclassical DBA should be ruled out and mutations of RP genes studied.