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J Pediatr Hematol Oncol ; 41(8): 644-647, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-30179993

RESUMO

Beta thalassemia major (ßTM) is the most common inherited hemoglobinopathy. Management essentially focuses on preventing and treating complications. Conventional treatment is based on a regular blood transfusion program, and chelation therapy. Management essentially focuses on preventing and treating complications. Severe complications of ßTM are very rarely seen in children in Europe. In the context of the migrant crisis, pediatricians will be confronted with the challenge of managing severe complicated ßTM. We report the case of 2 Syrian 10-year-old twin girls who arrived to France with numerous and severe complications of ßTM: hemochromatosis, alloimmunization, hypopituitarism, osteopenia… Their clinical management, which led to successful vital and functional improvement, is reported in this article.


Assuntos
Doenças Ósseas Metabólicas , Hemocromatose , Hipopituitarismo , Refugiados , Gêmeos , Talassemia beta , Doenças Ósseas Metabólicas/etiologia , Doenças Ósseas Metabólicas/patologia , Doenças Ósseas Metabólicas/terapia , Criança , Feminino , Hemocromatose/etiologia , Hemocromatose/patologia , Hemocromatose/terapia , Humanos , Hipopituitarismo/etiologia , Hipopituitarismo/patologia , Hipopituitarismo/terapia , Talassemia beta/complicações , Talassemia beta/patologia , Talassemia beta/terapia
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