alcaptonuria

[미국]/ˌælkæptəˈnjʊərɪə/
[영국]/ˌælkæptoʊˈnʊrɪə/

한국어 번역

Word Forms
복수형alcaptonurias

구문 및 연어

alcaptonuria patient

alcaptonuria diagnosis

alcaptonuria symptoms

alcaptonuria treatment

alcaptonuria test

alcaptonuria disease

alcaptonuria condition

alcaptonuria case

alcaptonuria research

alcaptonuria cause

예문

alcaptonuria is a rare genetic disorder that causes black urine.

the disease alcaptonuria leads to the accumulation of homogentisic acid.

patients with alcaptonuria often develop ochronosis in later life.

alcaptonuria can be diagnosed through urine testing.

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

alcaptonuria causes dark pigmentation in connective tissue.

classical alcaptonuria symptoms include dark urine and joint pain.

alcaptonuria is an inherited metabolic disorder affecting amino acid breakdown.

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

arthritis is a common complication of alcaptonuria in middle age.

genetic testing can confirm alcaptonuria in suspected cases.

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

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