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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.
Although an epicanthic fold can also be associated with a less prominent upper eyelid crease (a feature commonly termed "single eyelids" as opposed to "double eyelids"), the two features are distinct; a person may have both epicanthal folds and an upper eyelid crease, one and not the other, or neither. [2]
An epicanthic fold, the skin fold of the upper eyelid covering the inner corner (medial canthus) of the eye, may be present based on various factors, including ancestry, age, and certain medical conditions. In some populations the trait is almost universal, specifically in East Asians and Southeast Asians, where a majority, up to 90% in some ...
This page was last edited on 14 December 2024, at 19:54 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Please include a photo of a person who does not have an epicanthic fold, for comparison. That would allow the reader to more clearly compare the specific features that make up the fold. As it is, I see general features but still do not understand what the epicanthic fold is. -Pgan002 18:18, 30 October 2008 (UTC)
A cold-adaptive explanation for the epicanthic fold is today seen as outdated by some, as epicanthic folds appear in some African populations. Dr. Frank Poirier, a physical anthropologist at Ohio State University, concluded that the epicanthic fold in fact may be an adaptation for tropical regions , and was already part of the natural diversity ...
Retrieved from "https://en.wikipedia.org/w/index.php?title=Epicanthal_fold&oldid=711618042"This page was last edited on 23 March 2016, at 22:29 (UTC). (UTC).
Megalocornea-intellectual disability syndrome, also known as Neuhauser syndrome, is a very rare genetic disorder which is characterized by megalocornea, hypotonia from birth, variable intellectual disabilities, psychomotor delays, developmental delays, and facial dysmorphisms such as round face, frontal bossing, antimongoloid slants of the eyes, epicanthal fold, large, low-set ears, broad ...