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Objectiv: To probe the diagnostic and the prognostic values of adenine deaminase( ADA) in acute icterohepatitis and its role in curative effect.

目的了解血清ADA在急诊断、预后评估中的临床价值。

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featherback, featherbed, featherbedding, featherbone, featherboning, featherbrain, feather-brain, featherbrained, feathercut, feathered,

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Osmosis-血液肿瘤

From there, four molecules of Porphobilinogen condense together to form Hydroxymethylbilane with help of Porphobilinogen deaminase.

从这里开始,四胆色素原在胆色素原脱氨酶的作用下凝聚在起,形成羟甲基胆色烷。

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Osmosis-血液肿瘤

From there, four molecules of porphobilinogen condense together to form hydroxymethylbilane with the help of porphobilinogen deaminase.

卟胆原的四构成,羟甲基胆素在卟胆原脱氨酶的辅助下。

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Osmosis-血液肿瘤

Note that porphobilinogen deaminase is sometimes called uroporphyrinogen I synthase or hydroxymethylbilane synthase, or HMBS for short.

卟胆原脱氨酶有时被称为尿卟啉原I合成酶或羟甲基胆素合成酶,略为HMBS。

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Osmosis-血液肿瘤

The diagnosis is confirmed by measuring erythrocyte porphobilinogen deaminase activity.

可通过检测红细胞内卟胆原脱氨酶活性以确诊。

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Osmosis-血液肿瘤

The majority of individuals with the HMBS gene mutation and a deficiency of porphobilinogen deaminase are asymptomatic.

存在HMBS基因突变及缺乏卟胆原脱氨酶的人群大部没有症状。

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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。

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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。

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3G, 401(K), a,
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