alcaptonuria

[美]/ˌælkæptəˈnjʊərɪə/
[英]/ˌælkæptoʊˈnʊrɪə/

释义

n.尿黑酸尿
词形变化

短语搭配

alcaptonuria patient

黑尿症患者

alcaptonuria diagnosis

黑尿症诊断

alcaptonuria symptoms

黑尿症症状

alcaptonuria treatment

黑尿症治疗

alcaptonuria test

黑尿症检测

alcaptonuria disease

黑尿症疾病

alcaptonuria condition

黑尿症病情

alcaptonuria case

黑尿症病例

alcaptonuria research

黑尿症研究

alcaptonuria cause

黑尿症病因

例句

alcaptonuria is a rare genetic disorder that causes black urine.

尿黑症是一种罕见的遗传疾病,会导致尿液变黑。

the disease alcaptonuria leads to the accumulation of homogentisic acid.

尿黑症这种疾病会导致尿黑酸在体内积聚。

patients with alcaptonuria often develop ochronosis in later life.

尿黑症患者在晚年常会患上黄褐症。

alcaptonuria can be diagnosed through urine testing.

尿黑症可以通过尿液检测进行诊断。

there is currently no cure for alcaptonuria, only symptom management.

目前尿黑症无法治愈,只能进行症状管理。

alcaptonuria causes dark pigmentation in connective tissue.

尿黑症会导致结缔组织出现深色色素沉着。

classical alcaptonuria symptoms include dark urine and joint pain.

尿黑症的典型症状包括尿液变黑和关节疼痛。

alcaptonuria is an inherited metabolic disorder affecting amino acid breakdown.

尿黑症是一种影响氨基酸分解的遗传性代谢疾病。

the black urine associated with alcaptonuria is a distinctive diagnostic sign.

尿黑症伴随的黑尿是一个独特的诊断征象。

arthritis is a common complication of alcaptonuria in middle age.

关节炎是尿黑症在中年时期的常见并发症。

genetic testing can confirm alcaptonuria in suspected cases.

基因检测可以确诊疑似尿黑症病例。

alcaptonuria was one of the first metabolic disorders described in medical literature.

尿黑症是医学文献中最早描述的代谢疾病之一。

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