alkaptonurias

[US]/ˌæl.kæpˈtoʊnɪəri.əs/
[UK]/ˌæl.kæpˈtoʊniː.ər.i.əs/

Translation

n.A group of inherited metabolic disorders characterized by the inability to properly break down certain amino acids, leading to a buildup of homogentisic acid in the body which is excreted in urine, causing it to darken.

Phrases & Collocations

alkaptonurias research

rare alkaptonurias cases

alkaptonurias genetic testing

symptoms of alkaptonurias

alkaptonurias treatment options

understanding alkaptonurias

alkaptonurias patient support

living with alkaptonurias

Example Sentences

alkaptonurias is a rare genetic disorder.

the symptoms of alkaptonurias can vary widely.

alkaptonurias is characterized by the buildup of homogentisic acid in the body.

early diagnosis and treatment are crucial for alkaptonurias.

alkaptonurias can affect multiple organ systems.

research is ongoing to develop new treatments for alkaptonurias.

genetic testing can help identify individuals at risk for alkaptonurias.

alkaptonurias is a complex disorder that requires specialized care.

support groups can provide valuable information and emotional support to families affected by alkaptonurias.

living with alkaptonurias can present unique challenges.

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