血色病 的英文怎麼說

中文拼音 [xiěshǎibìng]
血色病 英文
hemachromatosis
  • : 血名詞(血液 多用於口語) blood:吐血 spit (up) blood; 血的教訓 a lesson paid for [written] in b...
  • : 色名詞[口語] (顏色) colour
  • : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • 血色 : redness of the skin; colour
  1. Figure 9. case 7. additional vessel ( purple ) behind the 4 - chamber view next to the aorta ( red ). this vessel represents an azygous or hemizygous continuation of an interrupted inferior vena cava

    圖9例7四腔心切面顯示靠近主動脈(紅)處的額外的一條靜脈(紫) 。這條管表示的是下腔靜脈中斷后在單側的延續。
  2. Kallner and groen studied the mortality from coronary heart disease and cerebrovascular accidents among immigrants to israel.

    Kallner和Groen研究了去以列的移民中的患冠心與腦管死亡率。
  3. In a series of 30 cases of retinitis pigmentosa, pigment epithelial alterations included mottling of the macula in 8 eyes ( 13. 3 % ), bull ' s - eye pattern in 24 eyes ( 40 % ) and atrophy or hypopigmentation in 56 eyes ( 93. 3 % ) ; macular edema with retinal thickening was present in 30 eyes ( 50 % ), cystoid macular edema in 18 eyes ( 30 % ) ; broadening or loss of foveal reflex was present in 60 eyes ( 100 % ), preretinal membrane noticed in 58 eyes ( 96. 7 % ) and macular hemorrhage in one eye ( 1. 7 % )

    摘要對網膜素變性癥的例30例60眼探討其黃斑部灶的情形,網膜素上皮層變化中的雜斑點變見於8眼,頻率為13 . 3 % ,牛眼樣灶見於24眼( 40 % ) ,網膜脫灶為56眼( 93 . 3 % ) ;黃斑部浮腫之網膜增厚為30眼( 50 % ) ,類囊胞浮腫為18眼( 30 % ) ;其它變化包括中心窩反射消失或增寬為60眼( 100 % ) ,網膜前纖維膜為58眼( 96 . 7 % ) ,黃斑部出和疑似網膜下新生管各為1眼( 1 . 7 % ) 。
  4. Figure 16. a, desmoid tumor in a previous scar. b, color doppler scan of a desmoid tumor in a previous scar revealing some vascularity in the lesion

    圖16 , a ,以前疤痕處的硬纖維瘤。 b ,彩多普勒掃描以前瘢痕處的硬纖維瘤變處顯示一些管供應。
  5. These diseases detected were esophageal varices, erosive gastritis, bile reflux gastritis, xanthoma, duodenitis, duodenal ulcer, small intestinal cancer, small intestinal angiodysplasia, crohn ' s disease, intestinal polyp, intestinal erosion and congestion, diverticula, colon melanosis and colonic cancer

    檢出了15種變:食道靜脈曲張、糜爛性胃炎、膽汁返流性胃炎、胃黃瘤、十二指腸炎、十二指腸潰瘍、小腸腫瘤、小腸管畸形、克羅恩、小腸單發及多發息肉、非特異性小腸炎、吸收不良綜合征、小腸憩室、結腸黑變、結腸癌。
  6. A large number of haemoptysis are phthisical patient ' s serious symptom, can jam because of many clot tracheal, make the patient appears asphyxial, expression balks for haemoptysis, appear bosom frowsty, be agitated, give cold sweat, even complexion empurples wait for a symptom, if cannot be handled in time, can endanger patient life

    大量咯是肺結核人嚴重的癥狀,可因大量的塊堵塞氣管,使人出現窒息,表現為咯忽然停止,並出現胸悶、煩躁、出冷汗,甚至面發紫等癥狀,假如不能及時處理,則可危及人生命。
  7. Part 1 : the culture and identification of es - d3 cells and the study of the efficiency of eb formation from es cells when grown on mef feeder layer in es culture medium or cultured in es culture medium supplemented with lif 1000u / ml, es - d3 cells being used in our experiments formed normal clones, expressed akp and kept their normal karyotype over many passages. the in vitro and in vivo differentiation experiments showed that es - d3 cells could differentiate into variety of cell types derived from three primary germ layers

    結果顯示: eso3細胞在小鼠胚胎成纖維細胞上和或含白抑制因於億f )的es細胞培養液中形成典型的胚胎幹細胞克隆,堿性磷酸酶染結果為強陽性,具有正常二倍體核型以及具有在體內外分化為三個胚層來源的組織細胞的潛能,而且具有形成種系嵌合動物的能力。
  8. Hhc results from a mutation involving the hemochromatosis gene ( hfe ) that leads to increased iron absorption from the gut

    是由於素沉著癥基因( hfe )突變使得腸吸收鐵增加所致。
  9. Metabolic diseases such as wilson ' s disease, hemochromatosis, and alpha 1 - antitrypsin deficiency can lead to liver damage

    代謝性疾,如威爾遜氏沉著, - 1型胰島素缺乏癥均可導致肝損傷。
  10. Metabolic diseases such as wilson ' s disease, hemochromatosis, and alpha 1 - antitrypsin deficiency can lead to liver damage

    代謝性疾,如威爾遜氏沉著, - 1型胰島素缺乏癥均可導致肝損傷。
  11. Hemochromatosis leads to bronze pigmentation of skin, diabetes mellitus ( from pancreatic involvement ), and cardiac arrhythmias ( from myocardial involvement )

    素沉著癥導致皮膚的青銅素沉著、糖尿(累及胰腺) 、心率失常(累及心肌) 。
  12. Hemochromatosis - a genetic disorder involving increased absorption of iron by the gastrointestinal tract and deposition in the liver resulting ultimately in cirrhosis and liver failure

    沉著? ?一種遺傳性癥引起胃腸道吸收鐵增多,沉積在肝臟,導致最終肝硬化或肝衰竭。
  13. Hemochromatosis can be primary ( the cause is probably an autosomal recessive genetic disease ) or secondary ( excess iron intake or absorption, liver disease, or numerous transfusions )

    素沉著癥或可以是原發的(因大概為常染體隱性遺傳) ,也可以是繼發的(過多的鐵攝取或吸收、肝臟疾、大量輸) 。
  14. But more and more studies showed that iron - overload was involved in many diseases ( such as atherosclerosis, ischemia / reperfusion injure, hereditary hemochromatosis, and so on )

    然而近來的研究發現,鐵超載在機體一些疾(如動脈粥樣硬化、心肌缺復灌性損傷、遺傳性)的發展過程中起了重要的作用。
  15. Early evaluation of lower limbs ' angiopathy by color doppler ultrasound in type 2 diabetic patients

    多普勒超聲對2型糖尿患者下肢變的早期評估價值
  16. Especially, those hereditary diseases of the alien brides deserre us to explore, such as - thalassemia and hemoglobin e

    尤其是外籍新娘的遺傳性疾值得我們去探討,如乙型海洋性貧素e癥。
  17. Does dominance hereditary disease have those ? recessive have those again

    像紅綠盲,白化都是隱性遺傳,六指就是顯性的
  18. It is applicable to patients with diabetes, cardio - cerebrovascular disease, wind dampness, rheumatoid disease, ankylosing spondylitis, anemia, climacteric syndrome, mottle and other syndromes with disordered endocrine, unbalanced metabolism and low immunity

    用於糖尿、心腦、風濕、類風濕、強直性脊柱炎、貧、更年期綜合癥、斑等內分泌失調、代謝紊亂、免疫力低下的人群。
  19. In 2001, wilson and his colleagues cloned another two members - human wnk1 gene and wnk4 gene which were located on chromosome 12 and 17, respectively. the two genes are disease - causing genes responsible for a mendelian hypertension. the disease - causing mutations are the large deletions in the first intron in wnk1 gene, causing increased expression in leukocytes

    2001年, wilson等克隆了此家族的另兩個成員? ?人的wnk1和wnk4基因,分別位於12號和17號染體,這兩個基因是一種孟德爾遺傳型高的致基因,致突變分別是wnk1基因第一內含子的大片段缺失,導致患者白細胞的基因表達量提高5倍左右。
  20. Observation on peripheral vessel lesions of 118 aged patients by color doppler ultrasound

    多普勒超聲對118例老年患者周圍變的觀察
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