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EntityQ1507609· pop 9· linked from 93 articles

ochronosis

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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.

In the Vinony graph

Vinony's link graph records 93 inbound references to ochronosis, and connects out to digital object identifier, phenol and albinism.

It sits within the topics Amino acid metabolism disorders, Autosomal recessive disorders and Skin conditions resulting from errors in metabolism.

Vinony links it to 8 Wikipedia language editions.

Research

1,178 papers

via PubMed

Wikidata facts

Subclass of
disease
Image
Homogentisic acid.svg
Show 6 more facts
NCI Thesaurus ID
C84938
health specialty
endocrinology
Commons category
Ochronosis
ICD-9-CM
270.2
on focus list of Wikimedia project
WikiProject Medicine
Sources (4)

via Wikidata · CC0

~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

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