必应词典为您提供alkaptonuria的释义,美[ɔ:lkæp'tʌnjʊərɪə],英[ɔ:lkæp'tʌnjʊərɪə],n. 尿黑酸尿; 网络释义: 黑尿症;尿黑酸症;尿黑酸尿症;
alkaptonuria 英[ɔ:lkæp'tʌnjʊərɪə] 美[ɔlkæp'tʌnjʊərɪr] 释义 尿黑酸尿 实用场景例句 全部 Thoracic myelopathy in a patient withalkaptonuriahas not been previously reported. 之前尚无尿黑酸尿病人合并胸椎脊髓病的报道....
alkaptonuria [美[ɔ:lkæp'tʌnjʊərɪr]] alkaptonuria的意思、解释 尿黑酸尿 网络尿黑酸尿症;尿黑酸症;尿黑酸尿;黑酸尿症 更多
黑尿症(alkaptonuria),又称黑尿病、黑尿酸症、伽罗德综合征,是人类的一种罕见常染色体隐性遗传代谢缺陷病,因病人的尿色发黑而得名,该病和酪氨酸和苯丙氨酸的代谢障碍有关,早期除了尿色发黑,多无表现,成年后会造成骨关节及脏器的损害。黑尿症发病率为百万分之一,英国...
尿黑酸尿症(Alkaptonuria,AKU)又称为黑尿症或褐黄病,是一种罕见的酪氨酸代谢障碍性疾病,呈常染色体隐性遗传,由编码尿黑酸1,2-二氧化酶的HGD基因(homogentisate 1,2 dioxygenase,HGD)突变所致。患者因先天缺乏尿黑酸氧化酶,导致体内苯丙氨酸和酪氨酸代谢产生的尿黑酸(homogentisic acid,HGA)无法降解,经尿液排出,...
Twitter Google Share on Facebook Thesaurus Medical Encyclopedia Wikipedia ThesaurusAntonymsRelated WordsSynonymsLegend: Switch tonew thesaurus Noun1. alkaptonuria- a rare recessive metabolic anomaly marked by ochronosis and the presence of alkapton in the urine ...
【疾病概述】疾病定义:尿黑酸尿症(Alkaptonuria,AKU)又称为黑尿症或褐黄病,是一种罕见的酪氨酸代谢障碍性疾病,呈常染色体隐性遗传,由编码尿黑酸1,2-二氧化酶的HGD基因(homogentisate 1,2 dioxygenase,HGD…
将“alkaptonuria"翻译成中文 黑尿症, 尿黑酸尿, 黑尿酸尿症是“alkaptonuria"到 中文 的最佳翻译。 alkaptonuria noun 语法 (medicine) A rare inherited genetic disorder of phenylalanine and tyrosine metabolism, causing the accumulation and eventual excretion of alkapton. [..] + 添加翻译 英文-...
The condition is also inherited. Which indeed means it passes on from the parents to their children. In case, both the parents tend to carry a defective gene which is related to alkaptonuria, then all of their children have a twenty five percent chance to develop the condition. ...
Alkaptonuria itself is asymptomatic, but the sclera of the eyes may be pigmented (often only at a later age)[1]and the skin is darkened in sun-exposed areas as well as around sweat glands; sweat may be coloured brown. Urine may turn brown on standing, especially when left for a period...