thalassemia的意思

thalassemia中文翻譯：

n.地中海貧血；庫利氏貧血

相似詞語短語

thalassemia E───地中海貧血

雙語使用場景

Yijie, a 4 year old girl, was diagnosed with thalassemia major when she was just four months old.───王藝潔，一個4歲的女孩，當在4個月大的時候就被診斷出重型地中海貧血病。

using umbilical blood detect the thalassemia to neonate.───應用臍血對新生兒進行地中海貧血的篩查。

Objective To investigate the clinical significance of automated reticulocyte multiple parameters analysis in thalassemia patients.───目的：探討網織紅細胞參數在地中海貧血檢測的臨床意義。

A pair of twin girls suffered from thalassemia major.───一對孿生姐妹嬰兒患上了重型地中海貧血。

Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume(MCV).───目的了解平均紅細胞體積（MCV）降低兒童的珠蛋白生成障礙貧血（地貧）基因攜帶率。

Evidence-based recommendations at present rely mainly on the data obtained from intermediate and major thalassemia studies.───當前的循證建議主要依賴中度與重度地中海貧血研究中得出的數據。

The thalassemia belt passes through the Mediterranean and West and Central Asian countries.───“地中海貧血癥”的分布，則由地中海地區延伸至西亞以及中亞各國。

He was also informed that, due to thalassemia gene deletion or mutation is caused by, but not its genetic transmission.───同時他還得知，地中海貧血由于是基因缺失或突變引起的，因此它遺傳但不傳染。

Free erythrocyte Protoporphyrin (FEP)were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.───測定116例珠蛋白生成障礙性貧血、37例缺鐵性貧血患者及45例正常人的FEP水平。

英語使用場景

Objective To investigate the carrier rate of thalassemia gene in children with decreased mean corpuscular volume(MCV).

Thalassemia is considered a kind of heritable hemolytic disease with high heterology.

Methods: Using man - vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet .

Mediterranean anemia(thalassemia), occurring relatively often in southern China, is a genetic and hemolytic disease induced by disfunction of globin synthesis.

Methods: Using mon-vessel screen method of thalassemia and relative value of G6PD detect thalassemia and G6PD deficiency for man and woman of detection of before marriage in 4268 duplet.

Objectives To evaluate the early diagnosis way of thalassemia major.

Diseases such as sickle cell anemia and beta thalassemia result from abnormal red blood cells and can be treated with bone-marrow transplants.

A pair of twin girls suffered from thalassemia major.

Free erythrocyte Protoporphyrin(FEP)were determined in 116 thalassemia patients, 37 iron deficiency anemia patients and 45 normal subjects.