Literature DB >> 16493623

Diamond-Blackfan anemia associated with beta-thalassemia trait.

Betül Tavil1, Mualla Cetin, Bariş Kuşkonmaz, Fatma Gümrük.   

Abstract

A 14-month-old boy was referred to our hospital for evaluation of severe anemia. In the bone marrow aspiration smear, normal cellularity with severe erythroblastopenia (3%) was observed. The hemoglobin electrophoresis of the patient and his father were compatible with the beta-thalassemia trait. Because macrocytosis of Diamond-Blackfan anemia (DBA) is masked by microcytosis of beta-thalassemia trait, the diagnosis of DBA co-existing with beta-thalassemia trait might be challenging. We report herein a case of DBA co-existing with beta-thalassemia trait in a Turkish boy.

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Year:  2006        PMID: 16493623     DOI: 10.1002/ajh.20530

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  2 in total

1.  Novel variants in Iranian individuals suspected to have inherited red blood cell disorders, including bone marrow failure syndromes.

Authors:  Maryam Neishabury; Maghsood Mehri; Zohreh Fattahi; Hossein Najmabadi; Azita Azarkeivan
Journal:  Haematologica       Date:  2019-05-16       Impact factor: 9.941

2.  [Diagnosis and therapeutic outcomes of 12 cases thalassemia with concomitant acquired bone marrow failure].

Authors:  S B Fan; J Shi; N Nie; Y Q Shao; Z D Huang; J Zhang; J B Huang; X X Li; M L Ge; Y Z Zheng
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2017-12-14
  2 in total

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