An epicanthic fold or epicanthus[6] is a skin fold of the upper eyelid that covers the inner corner (medial canthus) of the eye.[3] However, variation occurs in the nature of this feature and the possession of "partial epicanthic folds" or "slight epicanthic folds" is noted in the relevant literature.[7][8][9] Various factors influence whether epicanthic folds form, including ancestry, age, and certain medical conditions.
Etymology
Epicanthus means 'above the canthus', with epi-canthus being the Latinized form of the Ancient Greek ἐπίκανθός: 'corner of the eye'.
Classification
This image highlights the epicanthic folds in a person of East Asian descent.
Variation in the shape of the epicanthic fold has led to four types being recognised:
Epicanthus supraciliaris runs from the brow, curving downwards towards the lachrymal sac.
Epicanthus palpebralis begins above the upper tarsus and extends to the inferior orbital rim.
Epicanthus tarsalis originates at the upper eyelid crease and merges into the skin near the medial canthus. This is the type most often found in East Asians.
Epicanthus inversus runs from the lower eyelid skin over the medial canthus and extends to the upper lid.[10]
In some of these populations, the trait is almost universal. This is especially true in East Asians and Southeast Asians, where a majority, up to 90% in some estimations, of adults have this feature.[12]
Swedish ski racer Jens Byggmark with an epicanthic fold over his left eye.
The degree of development of the fold between individuals varies greatly, and attribution of its presence or absence is often subjective, being to a degree relative to the occurrence of the trait within the community of the specific observer. Also, its frequency varies but can be found in peoples all over the world. Its use, therefore, as a phenotypic marker to define biological populations is debatable.[9]
Possible evolutionary function
The epicanthic fold is often associated with greater levels of fat deposition around the eyeball. The adipose tissue is thought to provide greater insulation for the eye and sinuses from the effects of cold, especially from freezing winds, and to represent an adaptation to cold climates. It has also been postulated that the fold itself may provide a level of protection from snow blindness. Though its appearance in peoples of Southeast Asia can be linked to possible descent from cold-adapted ancestors, its occurrence in various African peoples is not open to this explanation. The epicanthic fold found in many African people has been tentatively linked to protection for the eye from the high levels of ultraviolet light found in desert and semi-desert areas.[18]
The exact evolutionary function and origin of epicanthic folds remains unknown. Scientific explanations include either random variation and selection (presumably sexual selection), or possible adaption to desert environment and/or high levels of ultraviolet light found in high-altitude environments, such as the Himalayas.
Dr. Frank Poirier, a physical anthropologist at Ohio State University, said that the epicanthic fold among Asian people is often explained as part of an adaptation to severe cold or tropical environments, however he suggests that neither of these explanations are sufficient to explain its presence in East and Southeast Asia, and notes that the fold can also be observed in Irish and African people. He attributes the epicanthic fold to pleiotrophic genes that control for more than one characteristic or function. He also did not offer an explanation for the origin of epicanthic folds.[19]
Other factors
The Khoisan and some other African groups have a high frequency of the epicanthic fold.
Age
Many fetuses lose their epicanthic folds after three to six months of gestation.[20] Epicanthic folds may be visible in the development stages of young children of any ethnicity, especially before the nose bridge fully develops.[21]
Medical conditions
Epicanthic fold prevalence can sometimes be found as a sign of congenital abnormality, such as in Zellweger syndrome[22] and Noonan syndrome. Medical conditions that cause the nasal bridge not to develop and project are also associated with epicanthic fold. About 60% of individuals with Down syndrome (also known as trisomy 21) have prominent epicanthic folds.[23][24] In 1862, John Langdon Down classified what is now called Down syndrome. He used the term mongoloid for the condition. This was derived from then-prevailing ethnic theory[25] and from his perception that children with Down syndrome shared physical facial similarities (epicanthic folds) with those of Blumenbach's Mongolian race. While the term "mongoloid" (also "mongol" or "mongoloid idiot") continued to be used until the early 1970s, it is now considered pejorative and inaccurate and is no longer in common use since the 1970s about such medical conditions.[26]
Other examples are fetal alcohol syndrome, phenylketonuria, and Turner syndrome.[27]
^Powell, M. L. (1981) Assessment and management of developmental changes and problems in children, Mosby, Incorporated, p. 38 ISBN9780801615207
^U. Schilbach, U. and Rott, H-D. (1988) Ocular Hypotelorism, Submucosal Cleft Palate, and Hypospadias: A New Autosomal Dominant Syndrome, American Journal of Medical Genetics 31, pp. 863–870
^"ORIGIN OF SHAPE OF ASIAN EYES IS STILL A MYSTERY TO SCIENTISTS". Chicago Tribune. "Dr. Frank Poirier, a physical anthropologist at Ohio State University, says the classical explanation of epicanthic fold depicts it as an adaptation to the tropical and arctic regions where many Asians live. The fold is described as a sun visor protecting the eyes from overexposure to ultraviolet radiation or as a blanket insulating them from the cold. According to Poirier, the problem with this theory is that a substantial portion of the Asian population evolved in areas outside of the tropical and arctic regions. In addition, he says epicanthic fold is not limited to Asians. John F. Kennedy had a variance of the fold and it is found among Europeans, especially the Irish, he said. It`s just less prevalent. The fold is also found among infants worldwide. Poirier attributes the fold to pleiotropic genes--single genes that control more than one characteristic or function--but he has no explanation for its origin."
^Kalyanasundaram, S.; et al. (2010). "Peroxisomal Disorder-Unusual Presentation as Failure to Thrive in Early Infancy". Indian Journal of Pediatrics. 77 (10): 1151–1152. doi:10.1007/s12098-010-0199-6. PMID20872098. S2CID5736554.
^Hammer, Gary, D.; McPhee, Stephen J. (2010). "Pathophysiology of Selected Genetic Diseases". Pathophysiology of Disease: An Introduction to Clinical Medicine (6 ed.). New York: McGraw-Hill Medical. ISBN978-0-07-162167-0.{{cite book}}: CS1 maint: multiple names: authors list (link)
^Pham, V. (2010). COMMON OTOLARYNGOLOGICAL CONGENITAL ABNORMALITIES. UTMB, Dept. of Otolaryngology. [1]Archived 6 October 2011 at the Wayback Machine