Now individuals with acute intermittent porphyria have a mutation of the HMBS gene which codes for the enzyme porphobilinogen deaminase.
急性间歇性卟啉病的患者存在HMBS基因的突变;该基因编码卟胆原脱氨酶。
单词 | Acute intermittent porphyria |
释义 |
Acute intermittent porphyria
原声例句
Osmosis-血液肿瘤 Now individuals with acute intermittent porphyria have a mutation of the HMBS gene which codes for the enzyme porphobilinogen deaminase. 急性间歇性卟啉病的患者存在HMBS基因的突变;该基因编码卟胆原脱氨酶。 Osmosis-血液肿瘤 Glucose and heme are the treatments for acute intermittent porphyria as they inhibit aminolevulinic acid synthase, the first enzyme involved in heme synthesis. 葡萄糖和血红素用于治疗急性间歇性卟啉病,他们能抑制氨基乙酰丙酸的合成,即影响参与血红素合成的第一种酶。 Osmosis-血液肿瘤 To diagnose acute intermittent porphyria, a urinalysis is conducted which typically shows an elevation of porphobilinogen at least five times greater than normal levels. 为诊断急性间歇性卟啉病,尿检通常显示卟胆原水平上升,至少比正常值升高五倍。 Osmosis-血液肿瘤 So, the symptoms of acute intermittent porphyria can be remembered with the 4 P's mnemonic: Painful Abdomen, Polyneuropathy, Psychological disturbances, and Port-wine colored urine. 急性间歇性卟啉病的症状可以用4个P来记忆:腹痛、多发性神经病、精神障碍、葡萄酒色尿。 Osmosis-血液肿瘤 All right, as a quick recap, acute intermittent porphyria is an autosomal dominant disorder caused by a deficiency of the enzyme porphobilinogen deaminase in the heme synthesis pathway. 好,快速回顾一下:急性间歇性卟啉病是常染色体显性疾病,由血红素合成途径中缺乏卟胆原脱氨酶导致。 Osmosis-血液肿瘤 In order to better understand acute intermittent porphyria, we need to first take a look at hemoglobin, the main protein within red blood cells that's responsible for carrying oxygen. 为了更好地理解急性间歇性卟啉病,我们首先需要来了解血红蛋白;作为红细胞内的主要蛋白,它负责携带氧气。 Osmosis-血液肿瘤 The last important thing to keep in mind is that acute intermittent porphyria can be distinguished from the other many porphyrias by the fact that it doesn't cause any photosensitive cutaneous symptoms, like skin blistering when exposed to sunlight. 还需要牢记的是,急性间歇性卟啉病患者一般没有光敏皮肤症状,可区别与许多其他类型的卟啉病:那些患者暴露在光照下时,皮肤会起水疱。
英语百科
Acute intermittent porphyria![]() Acute intermittent porphyria (AIP) is a rare autosomal dominant metabolic disorder affecting the production of heme, the oxygen-binding prosthetic group of hemoglobin. It is characterized by a deficiency of the enzyme porphobilinogen deaminase. Acute intermittent porphyria is the second most common form of porphyria (porphyria cutanea tarda being the most common). Its incidence is estimated to be between 5 and 10 in 100,000, but this is likely underestimated because of positive cases not being induced, and long periods of latency, with an estimation that it is latent in 90% of cases. |
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