Heterochromia is a variation in coloration. The term is most often used to describe color differences of the iris, but can also be applied to color variation of hair or skin. Heterochromia is determined by the production, delivery, and concentration of melanin (a pigment). It may be inherited, or caused by genetic mosaicism, chimerism, disease, or injury. It occurs in humans and certain breeds of domesticated animals.
|Domestic cat with complete heterochromia|
|Symptoms||different or partially different eye colour|
|Treatment||iris implant surgery (controversial for cosmetic purposes)|
Heterochromia of the eye is called heterochromia iridum or heterochromia iridis. It can be complete or sectoral. In complete heterochromia, one iris is a different color from the other. In sectoral heterochromia, part of one iris is a different color from its remainder. In central heterochromia, there is a ring around the pupil or possibly spikes of different colors radiating from the pupil.
Though multiple causes have been posited, the scientific consensus is that a lack of genetic diversity is the primary reason behind heterochromia, at least in domestic animals. This is due to a mutation of the genes that determine melanin distribution at the 8-HTP pathway, which usually only become corrupted due to chromosomal homogeneity. Though common in some breeds of cats, dogs, cattle and horses, due to inbreeding, heterochromia is uncommon in humans, affecting fewer than 200,000 people in the United States, and is not associated with lack of genetic diversity.
The affected eye may be hyperpigmented (hyperchromic) or hypopigmented (hypochromic). In humans, an increase of melanin production in the eyes indicates hyperplasia of the iris tissues, whereas a lack of melanin indicates hypoplasia. The term is from Ancient Greek: ἕτερος, héteros 'different' and χρῶμα, chrôma 'color'.
Background - How eye color is determinedEdit
Eye color, specifically the color of the irises, is determined primarily by the concentration and distribution of melanin. Although the processes determining eye color are not fully understood, it is known that inherited eye color is determined by multiple genes. Environmental or acquired factors can alter these inherited traits.
The color of the mammalian, including human, iris is very variable. However, there are only two pigments present, eumelanin and pheomelanin. The overall concentration of these pigments, the ratio between them, variation in the distribution of pigment in the layers of the stroma of the iris and the effects of light scattering all play a part in determining eye color.
Heterochromia is classified primarily by onset: as either genetic or acquired. Although a distinction is frequently made between heterochromia that affects an eye completely or only partially (sectoral heterochromia), it is often classified as either genetic (due to mosaicism or congenital) or acquired, with mention as to whether the affected iris or portion of the iris is darker or lighter. Most cases of heterochromia are hereditary, or caused by genetic factors such as chimerism, and are entirely benign and unconnected to any pathology, however, some are associated with certain diseases and syndromes. Sometimes one eye may change color following disease or injury.
Sectoral or partial heterochromiaEdit
In sectoral heterochromia, sometimes referred to as partial heterochromia, areas of the same iris contain two completely different colors. It is unknown how rare sectoral heterochromia is in humans.
Abnormal Iris DarkerEdit
- Lisch nodules – iris hamartomas seen in neurofibromatosis.
- Ocular melanosis – a condition characterized by increased pigmentation of the uveal tract, episclera, and anterior chamber angle.
- Oculodermal melanocytosis (nevus of Ota)
- Pigment dispersion syndrome – a condition characterized by loss of pigmentation from the posterior iris surface which is disseminated intraocularly and deposited on various intraocular structures, including the anterior surface of the iris.[medical citation needed]
- Sturge–Weber syndrome – a syndrome characterized by a port-wine stain nevus in the distribution of the trigeminal nerve, ipsilateral leptomeningeal angiomas with intracranial calcification and neurologic signs, and angioma of the choroid, often with secondary glaucoma.
Abnormal Iris LighterEdit
- Simple heterochromia – a rare condition characterized by the absence of other ocular or systemic problems. The lighter eye is typically regarded as the affected eye as it usually shows iris hypoplasia. It may affect an iris completely or only partially.
- Congenital Horner's syndrome – sometimes inherited, although usually acquired.
- Waardenburg syndrome – a syndrome in which heterochromia is expressed as a bilateral iris hypochromia in some cases. A Japanese review of 11 children with albinism found that the condition was present. All had sectoral/partial heterochromia.
- Piebaldism – similar to Waardenburg's syndrome, a rare disorder of melanocyte development characterized by a white forelock and multiple symmetrical hypopigmented or depigmented macules.
- Hirschsprung's disease – a bowel disorder associated with heterochromia in the form of a sector hypochromia. The affected sectors have been shown to have reduced numbers of melanocytes and decreased stromal pigmentation.
- Incontinentia pigmenti
- Parry–Romberg syndrome
Acquired heterochromia is usually due to injury, inflammation, the use of certain eyedrops that damage the iris, or tumors.
Abnormal Iris DarkerEdit
- Deposition of material
- Certain eyedrops – prostaglandin analogues (latanoprost, isopropyl unoprostone, travoprost, and bimatoprost) are used topically to lower intraocular pressure in glaucoma patients. A concentric heterochromia has developed in some patients applying these drugs. The stroma around the iris sphincter muscle becomes darker than the peripheral stroma. A stimulation of melanin synthesis within iris melanocytes has been postulated.[medical citation needed]
- Neoplasm – Nevi and melanomatous tumors.
- Iridocorneal endothelium syndrome
- Iris ectropion syndrome
Abnormal Iris LighterEdit
- Fuchs heterochromic iridocyclitis – a condition characterized by a low grade, asymptomatic uveitis in which the iris in the affected eye becomes hypochromic and has a washed-out, somewhat moth eaten appearance. The heterochromia can be very subtle, especially in patients with lighter colored irides. It is often most easily seen in daylight. The prevalence of heterochromia associated with Fuchs has been estimated in various studies with results suggesting that there is more difficulty recognizing iris color changes in dark-eyed individuals.
- Acquired Horner's syndrome – usually acquired, as in neuroblastoma, although sometimes inherited.
- Neoplasm – Melanomas can also be very lightly pigmented, and a lighter colored iris may be a rare manifestation of metastatic disease to the eye.
- Parry–Romberg syndrome – due to tissue loss.
Central heterochromia is an eye condition where there are two colors in the same iris; the central (pupillary) zone of the iris is a different color than the mid-peripheral (ciliary) zone.
Central heterochromia is more noticeable in irises containing low amounts of melanin.
Heterochromia of the eye was described by Aristotle, who termed it heteroglaucos. Notable historical figures thought to have heterochromia include the Byzantine emperor Anastasius the First, dubbed dikoros (Greek for 'having two irises'). The Alexander Romance attributes heterochromia to Alexander the Great, who is described as having one eye light and one eye dark.
In other animalsEdit
Although infrequently seen in humans, complete heterochromia is more frequently observed in species of domesticated mammals, where it almost always involves one blue eye. The blue eye occurs within a white spot, where melanin is absent from the skin and hair (see Leucism). These species include the cat, particularly breeds such as Turkish Van, Turkish Angora, Khao Manee and (rarely) Japanese Bobtail. These so-called odd-eyed cats are white, or mostly white, with one normal eye (copper, orange, yellow, green), and one blue eye. Among dogs, complete heterochromia is seen often in the Siberian Husky and few other breeds, usually Australian Shepherd and Catahoula Leopard Dog and rarely in Shih Tzu. Horses with complete heterochromia have one brown and one white, gray, or blue eye—complete heterochromia is more common in horses with pinto coloring. Complete heterochromia occurs also in cattle and even water buffalo. It can also be seen in ferrets with Waardenburg syndrome, although it can be very hard to tell at times as the eye color is often a midnight blue.
Sectoral heterochromia, usually sectoral hypochromia, is often seen in dogs, specifically in breeds with merle coats. These breeds include the Australian Shepherd, Border Collie, Collie, Shetland Sheepdog, Welsh Corgi, Pyrenean Shepherd, Mudi, Beauceron, Catahoula Cur, Dunker, Great Dane, Dachshund and Chihuahua. It also occurs in certain breeds that do not carry the merle trait, such as the Siberian Husky and rarely, Shih Tzu. There are examples of cat breeds that have the condition such as Van cat.
Actress Alice Eve has heterochromia: her left eye is blue and right eye is grey.
Former cricketer Shane Warne has complete heterochromia.
Actress Kate Bosworth has sectoral heterochromia.
Actor Dominic Sherwood has sectoral heterochromia.
Actor Henry Cavill has sectoral heterochromia.
Complete heterochromia in a Siberian Husky: one eye blue, one eye brown.
Sectoral hypochromia in a blue merle Border Collie.
- Kumar P (2017). "Focal Scalp Hair Heterochromia in an Infant". Sultan Qaboos University Medical Journal. 17 (1): e116–118. doi:10.18295/squmj.2016.17.01.022. PMC 5380409. PMID 28417041.
- Imesch PD, Wallow IH, Albert DM (February 1997). "The color of the human eye: a review of morphologic correlates and of some conditions that affect iridial pigmentation throughout life". Survey of Ophthalmology. 41 (Suppl 2): S117–23. doi:10.1016/S0039-6257(97)80018-5. PMID 9154287.
- Loewenstein, John; Scott Lee (2004). Ophthalmology: Just the Facts. New York: McGraw-Hill. ISBN 0-07-140332-9.
- Konovalova EN, Gladyr EA, Kostiunina OV, Zinovieva LK (2017). "Congenital Defects of Beef Cattle and General Principles of their Prevention". Journal of Agriculture and Environment. doi:10.23649/jae.2017.2.3.1.CS1 maint: multiple names: authors list (link)
- Ur Rehman H (2008). "Heterochromia". CMAJ. 179 (5): 447–448. doi:10.1503/cmaj.070497. PMC 2518194. PMID 18725617.
- "heterochromia iridis - definition of heterochromia iridis in the Medical dictionary - by the Free Online Medical Dictionary, Thesaurus and Encyclopedia". Medical-dictionary.thefreedictionary.com. Retrieved 2014-04-27.
- Wielgus AR, Sarna T (December 2005). "Melanin in human irides of different color and age of donors". Pigment Cell Research. 18 (6): 454–64. doi:10.1111/j.1600-0749.2005.00268.x. PMID 16280011.
- Prota G, Hu DN, Vincensi MR, McCormick SA, Napolitano A (September 1998). "Characterization of melanins in human irides and cultured uveal melanocytes from eyes of different colors". Experimental Eye Research. 67 (3): 293–9. doi:10.1006/exer.1998.0518. PMID 9778410.
- Swann P. "Heterochromia." Archived 2006-01-08 at the Wayback Machine Optometry Today. January 29, 1999. Retrieved November 1, 2006.
- "Heterochromia: MedlinePlus Medical Encyclopedia". Nlm.nih.gov. Retrieved 2014-04-27.
- Gladstone RM (1969). "Development and Significance of Heterochromia of the Iris". Arch Neurol. 21 (2): 184–192. doi:10.1001/archneur.1969.00480140084008. PMID 5797351.
- Guha M, Maity D (2014). "Heterochromia iridis - a case study". Explor Anim Med Res. 4 (2): 240–245.
- "Heterochromia iridis". Genetic and Rare Diseases Information Center (GARD) – an NCATS Program. NIH. 8 April 2015. Retrieved 9 February 2019.
- van Emelen C, Goethals M, Dralands L, Casteels I (Jan–Feb 2000). "Treatment of glaucoma in children with Sturge-Weber syndrome". Journal of Pediatric Ophthalmology and Strabismus. 37 (1): 29–34. PMID 10714693.
- "Sturge-Weber syndrome: Definition and Much More from Answers.com". Answers.com<!. Retrieved 2009-11-19.
- Wallis DH, Granet DB, Levi L (June 2003). "When the darker eye has the smaller pupil". Journal of American Association for Pediatric Ophthalmology and Strabismus. 7 (3): 215–6. doi:10.1016/S1091-8531(02)42020-4. PMID 12825064.
- Ohno N, Kiyosawa M, Mori H, Wang WF, Takase H, Mochizuki M (Jan–Feb 2003). "Clinical findings in Japanese patients with Waardenburg syndrome type 2". Japanese Journal of Ophthalmology. 47 (1): 77–84. doi:10.1016/S0021-5155(02)00629-9. PMID 12586183.
- Brazel SM, Sullivan TJ, Thorner PS, Clarke MP, Hunter WS, Morin JD (February 1992). "Iris sector heterochromia as a marker for neural crest disease". Archives of Ophthalmology. 110 (2): 233–5. doi:10.1001/archopht.1992.01080140089033. PMID 1736874.
- Liu CSC (August 1999). "A case of acquired iris depigmentation as a possible complication of levobunolol eye drops". British Journal of Ophthalmology. 83 (12): 1405–6. doi:10.1136/bjo.83.12.1403c. PMC 1722884. PMID 10660314.
- Yang P, Fang W, Jin H, Li B, Chen X, Kijlstra A (March 2006). "Clinical features of Chinese patients with Fuchs' syndrome". Ophthalmology. 113 (3): 473–80. doi:10.1016/j.ophtha.2005.10.028. PMID 16458965.
- Arellanes-Garcia L, del Carmen Preciado-Delgadillo M, Recillas-Gispert C (June 2002). "Fuchs' heterochromic iridocyclitis: clinical manifestations in dark-eyed Mexican patients". Ocular Immunology and Inflammation. 10 (2): 125–31. doi:10.1076/ocii.10.2.125.13976. PMID 12778348. S2CID 21171244.
- Tabbut BR, Tessler HH, Williams D (December 1988). "Fuchs' heterochromic iridocyclitis in blacks". Archives of Ophthalmology. 106 (12): 1688–90. doi:10.1001/archopht.1988.01060140860027. PMID 3196209.
- Bloch-Michel E (1983). "Fuchs heterochromic cyclitis: current concepts". Journal Français d'Ophtalmologie (in French). 6 (10): 853–8. PMID 6368659.
- Mehta K, Haller JO, Legasto AC (2003). "Imaging neuroblastoma in children". Critical Reviews in Computed Tomography. 44 (1): 47–61. doi:10.1080/10408370390808469. PMID 12627783.
- Genetic and Rare Diseases Information Center (GARD). "Heterochromia iridis".
- Khan AO, Aldamesh M (June 2006). "Bilateral Duane syndrome and bilateral aniridia". Journal of American Association for Pediatric Ophthalmology and Strabismus. 10 (3): 273–4. doi:10.1016/j.jaapos.2006.02.002. PMID 16814183.
- Shauly Y, Weissman A, Meyer E (May–Jun 1993). "Ocular and systemic characteristics of Duane syndrome". Journal of Pediatric Ophthalmology and Strabismus. 30 (3): 178–83. PMID 8350229.
- Baldwin, Barry (1981). "Physical Descriptions of Byzantine Emperors". Byzantion. 51 (1): 8–21. ISSN 0378-2506. JSTOR 44170668.
- Fronimopoulos, John; Lascaratos, John (1992-03-01). "Some Byzantine chroniclers and historians on ophthalmological topics". Documenta Ophthalmologica. 81 (1): 121–132. doi:10.1007/BF00155022. ISSN 1573-2622. PMID 1473460. S2CID 26240821.
- Nawotka, Krzysztof (2010) Alexander the Great, Cambridge Scholarship Publishing, ISBN 9781443818117, p. 44
- Misk NA, Semieka MA, Fathy A (1998). "Heterochromia iridis in water buffaloes (Bubalus bubalis)". Veterinary Ophthalmology. 1 (4): 195–201. doi:10.1046/j.1463-5224.1998.00036.x. PMID 11397231.
- Hunt, Kevin (January 11, 2016). "The remarkable story behind David Bowie's most iconic feature". The Conversation. Retrieved January 17, 2016.
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