Question 1: In 2008, in ________, a baby was selectively implanted in order to be a cure for his brother's thalassemia. | |||
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Question 2: In Europe, the highest concentrations of the disease are found in ________ and in parts of Italy, in particular, Southern Italy and the lower Po valley. | |||
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Question 3: The child was born from an embryo screened to be free of the disease before implantation with ________. | |||
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Question 4: This is probably by making the red blood cells more susceptible to the less lethal species Plasmodium vivax, simultaneously making the host's red blood cell (RBC) environment unsuitable for the merozoites of the more lethal strain ________. | |||
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Question 5: Thalassemia is a quantitative problem of too few globins synthesized, whereas ________ (a hemoglobinopathy) is a qualitative problem of synthesis of an incorrectly functioning globin. | |||
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Question 6: There are also prevalences in descendants of people from ________ and Mediterranean countries (e.g. | |||
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Question 7: Thalassemia patients produce a deficiency of either α or β globin, unlike ________ which produces a specific mutant form of β globin. | |||
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Question 8: Treatment for patients with thalassemia major includes chronic ________ therapy, iron chelation, splenectomy, and allogeneic hematopoietic transplantation. | |||
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Question 9: There are an estimated 1,000 people living with ________ in the United States and an unknown number of carriers. | |||
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Question 10: ________, Italy, Portugal, Spain, and others). | |||
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