Rahbar S, Azizi M, Nowzari G
Acta Haematol. 1975;53(1):60-4. doi: 10.1159/000208157.
Homozygous haemoglobin LeporeBoston disease is described in an Iranian 16-year-old boy presenting the clinical manifestations of BETA-thalassaemia major. The parents were related (cousins), and both carriers of Lepore trait. It seems that the symptoms are milder in this case than what reported before.
一名16岁伊朗男孩被诊断为纯合子血红蛋白Lepore波士顿病，表现出重型β地中海贫血的临床表现。其父母为近亲（表亲），均携带Lepore特质。在这种情况下，症状似乎比之前报道的要轻。
