Homogentistic acid:

Correct answer: C. Alkaptonuria

  • A. Transcription
  • B. Nucleosomes
  • C. Alkaptonuria
  • D. Metacentric

Explanation

Homogentistic acid is an intermediate in the metabolism of tyrosine and phenylalanine. In individuals with alkaptonuria, a genetic disorder, homogentisic acid accumulates in the body due to a deficiency in the enzyme homogentisate 1,2-dioxygenase, leading to its excretion in urine and various health issues including dark pigmentation of connective tissues.

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