伊朗一例纯合子血红蛋白Lepore波士顿型病例。
A case of homozygous haemoglobin Lepore Boston in Iran.
作者信息
Rahbar S, Azizi M, Nowzari G
出版信息
Acta Haematol. 1975;53(1):60-4. doi: 10.1159/000208157.
PMID:807077
Abstract
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.
摘要
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。
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引用本文的文献
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Haemoglobin LeporeBoston in a Turkish family.一个土耳其家庭中的波士顿血红蛋白Lepore
J Med Genet. 1976 Oct;13(5):363-5. doi: 10.1136/jmg.13.5.363.
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