Skip to content
EntityQ1507609· pop 9· linked from 93 articles

ochronosis

Sign in to save

Also known as Ochronosis (disorder)

thumb|Ocher pigment, after which the condition was named, due to the similar color of affected tissue Ochronosis is a medical condition characterized by the accumulation of homogentisic acid in connective tissues, leading to pigmentation changes. The term derives from the yellowish-brown (ocher-like) discoloration observed in histological samples. However, macroscopically, the affected tissues often appear bluish-grey due to the Tyndall effect, a phenomenon in which scattered light gives deeper-lying pigments a blue hue.

Research

1,178 papers

via PubMed

~7 min read

Encyclopedic overview

9 sections
Contents
  • Types
  • Signs and symptoms
  • Causes
  • Pathophysiology
  • Diagnosis
  • Treatment
  • See also
  • References
  • External links

thumb|Ocher pigment, after which the condition was named, due to the similar color of affected tissue Ochronosis is a medical condition characterized by the accumulation of homogentisic acid in connective tissues, leading to pigmentation changes. The term derives from the yellowish-brown (ocher-like) discoloration observed in histological samples. However, macroscopically, the affected tissues often appear bluish-grey due to the Tyndall effect, a phenomenon in which scattered light gives deeper-lying pigments a blue hue.

Ochronosis is most commonly associated with the rare metabolic disorder alkaptonuria, a genetic condition involving homogentisic acid oxidase deficiency. It may also occur as an acquired condition, known as *exogenous ochronosis*, resulting from prolonged topical application or systemic exposure to certain phenol derivatives, particularly hydroquinone.

Excerpted from Wikipedia’s “ochronosis” article, available under the CC BY-SA 4.0 licence.

Available in 8 languages

via Wikidata sitelinks · CC0