alkapton Sentence Examples

  1. Alkaptonuria is a rare genetic disorder characterized by the accumulation of homogentisic acid, also known as alkapton, in the body.
  2. The presence of alkapton in the urine of individuals with alkaptonuria causes a dark discoloration upon exposure to air, turning the urine black.
  3. Alkaptonuria is an autosomal recessive condition, meaning that both parents must carry the gene for a child to inherit the disorder.
  4. The enzymatic deficiency in alkaptonuria results in the inability to metabolize tyrosine properly, leading to the accumulation of alkapton in various tissues.
  5. Ochronosis is a term used to describe the deposition of alkapton in connective tissues, causing dark pigmentation in cartilage, tendons, and other structures.
  6. Individuals with alkaptonuria may experience joint problems due to the deposition of alkapton in the joints, leading to arthritis-like symptoms.
  7. Alkaptonuria is typically diagnosed through urine tests that reveal the presence of homogentisic acid, and genetic testing can confirm the genetic mutation responsible.
  8. Management of alkaptonuria often involves a low-protein diet to reduce the intake of tyrosine, which can contribute to alkapton accumulation.
  9. Research is ongoing to explore potential treatments for alkaptonuria, including enzyme replacement therapy and gene therapy approaches.
  10. Early detection and management of alkaptonuria are crucial in preventing complications associated with the accumulation of alkapton in tissues and joints.

alkapton Meaning

Wordnet

alkapton (n)

an acid formed as an intermediate product of the metabolism of tyrosine and phenylalanine

Synonyms & Antonyms of alkapton

No Synonyms and anytonyms found

FAQs About the word alkapton

an acid formed as an intermediate product of the metabolism of tyrosine and phenylalanine

No synonyms found.

No antonyms found.

Alkaptonuria is a rare genetic disorder characterized by the accumulation of homogentisic acid, also known as alkapton, in the body.

The presence of alkapton in the urine of individuals with alkaptonuria causes a dark discoloration upon exposure to air, turning the urine black.

Alkaptonuria is an autosomal recessive condition, meaning that both parents must carry the gene for a child to inherit the disorder.

The enzymatic deficiency in alkaptonuria results in the inability to metabolize tyrosine properly, leading to the accumulation of alkapton in various tissues.