thalassemia major
地中海貧血重大
thalassemia minor
地中海貧血輕度
thalassemia trait
地中海貧血特徵
alpha thalassemia
α地中海貧血
beta thalassemia
β地中海貧血
thalassemia screening
地中海貧血篩查
thalassemia test
地中海貧血檢測
thalassemia carrier
地中海貧血攜帶者
thalassemia diagnosis
地中海貧血診斷
thalassemia patient
地中海貧血患者
thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
地中海貧血是一種遺傳性血液疾病，特徵是血紅蛋白生成異常。
many people are unaware they carry the thalassemia gene until their child is diagnosed.
許多人都不知道自己攜帶地中海貧血基因，直到孩子被診斷出此病。
regular blood transfusions are essential for patients with thalassemia major.
對於重度地中海貧血患者來說，定期輸血是必不可少的。
prenatal screening can detect thalassemia in unborn babies with high accuracy.
產前篩查可以高準確度檢測出未出生嬰兒是否患有地中海貧血。
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
鐵過載是地中海貧血患者的一種嚴重併發症，需要螯合療法。
thalassemia carrier screening is recommended for couples planning to start a family.
建議計劃要孩子的夫妻接受地中海貧血攜帶者篩查。
the severity of thalassemia depends on how many mutated genes a person inherits.
地中海貧血的嚴重程度取決於一個人繼承了多少個突變基因。
advances in gene therapy offer new hope for curing thalassemia in the future.
基因治療的進展為未來治療地中海貧血帶來了新的希望。
thalassemia intermedia patients experience moderate symptoms compared to the major form.
與重度地中海貧血相比，中度地中海貧血患者的症狀較為輕微。
children with thalassemia major often require lifelong medical care and support.
患有重度地中海貧血的兒童通常需要終身的醫療照顧和支持。
genetic counseling helps families understand the risks of passing thalassemia to their children.
遺傳諮詢幫助家庭了解將地中海貧血傳給孩子的風險。
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
地中海貧血在地中海、非洲和東南亞人群中最為普遍。
thalassemia major
地中海貧血重大
thalassemia minor
地中海貧血輕度
thalassemia trait
地中海貧血特徵
alpha thalassemia
α地中海貧血
beta thalassemia
β地中海貧血
thalassemia screening
地中海貧血篩查
thalassemia test
地中海貧血檢測
thalassemia carrier
地中海貧血攜帶者
thalassemia diagnosis
地中海貧血診斷
thalassemia patient
地中海貧血患者
thalassemia is a hereditary blood disorder characterized by abnormal hemoglobin production.
地中海貧血是一種遺傳性血液疾病，特徵是血紅蛋白生成異常。
many people are unaware they carry the thalassemia gene until their child is diagnosed.
許多人都不知道自己攜帶地中海貧血基因，直到孩子被診斷出此病。
regular blood transfusions are essential for patients with thalassemia major.
對於重度地中海貧血患者來說，定期輸血是必不可少的。
prenatal screening can detect thalassemia in unborn babies with high accuracy.
產前篩查可以高準確度檢測出未出生嬰兒是否患有地中海貧血。
iron overload is a serious complication that requires chelation therapy in thalassemia patients.
鐵過載是地中海貧血患者的一種嚴重併發症，需要螯合療法。
thalassemia carrier screening is recommended for couples planning to start a family.
建議計劃要孩子的夫妻接受地中海貧血攜帶者篩查。
the severity of thalassemia depends on how many mutated genes a person inherits.
地中海貧血的嚴重程度取決於一個人繼承了多少個突變基因。
advances in gene therapy offer new hope for curing thalassemia in the future.
基因治療的進展為未來治療地中海貧血帶來了新的希望。
thalassemia intermedia patients experience moderate symptoms compared to the major form.
與重度地中海貧血相比，中度地中海貧血患者的症狀較為輕微。
children with thalassemia major often require lifelong medical care and support.
患有重度地中海貧血的兒童通常需要終身的醫療照顧和支持。
genetic counseling helps families understand the risks of passing thalassemia to their children.
遺傳諮詢幫助家庭了解將地中海貧血傳給孩子的風險。
thalassemia is most prevalent in mediterranean, african, and southeast asian populations.
地中海貧血在地中海、非洲和東南亞人群中最為普遍。
探索常見搜尋詞彙