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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.
An anatomical variation in humans occurs in the creases and folds of the upper eyelid. 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 ...
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]
epicanthic fold is not unheard of in scottish peoples, this may be due to gentic backgrounds involving scythians via the pictish people or from the 5000 sarmation shoulder brought in by the romans. I have epicanthic fold as do many of my male relatives and Im scottish descent. Some of my relatives also have exhibited mongolian spot.
The lacrimal caruncle is found at the medial canthus of the eye. [1] It consists of skin, hair follicles, sebaceous glands, sweat glands, accessory lacrimal tissue and other tissues that are present in the skin and accessory lacrimal glands.
The fissure may be increased in vertical height in Graves' disease, which is manifested as Dalrymple's sign.It is seen in disorders such as cri-du-chat syndrome. In animal studies using four times the therapeutic concentration of the ophthalmic solution latanoprost, the size of the palpebral fissure can be increased.
Accessory soleus muscle; Axillary arch; Epitrochleoanconeus muscle - or anconeous epitrochlearis; Extensor medii proprius muscle; Extensor digitorum brevis manus muscle; Extensor indicis et medii communis muscle
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 ...