Are Epicanthal folds normal in babies?

Are Epicanthal folds normal in babies?

Epicanthal folds are the folds of skin that run from the upper eyelid to the inner corner of the eye. In some people, they cover this inner corner. This is completely normal in many people, including those of Asian descent and infants.

When do Epicanthal folds go away?

Age. Many fetuses lose their epicanthic folds after three to six months of gestation. Epicanthic folds may be visible in the development stages of young children of any ethnicity, especially before the nose bridge fully develops.

What is a Mongolian fold?

Mongolian or epicanthal folds are skin folds of the upper eyelids that cover the inner corner of the eyes, resulting in the characteristic Asian appearance.

Why does my baby have Epicanthal folds?

Epicanthal folds may be normal for people of Asiatic descent and some non-Asian infants. Epicanthal folds also may be seen in young children of any race before the bridge of the nose begins to rise. However, they may also be due to certain medical conditions, including: Down syndrome.

What does Epicanthal folds mean?

An epicanthal fold is a skin fold of the upper eyelid covering the inner corner of the eye. It is often seen as a normal finding in very young children and is also common in people of Asiatic decent. An epicanthal fold can be an important diagnostic finding in conditions such as Down syndrome.

Do Epicanthal folds affect vision?

It gives the eyelid the appearance of having no crease. 1 In some cases, it can make the eyelid more prominent and droopy, creating a more narrow appearance in the eye. Monolids are perfectly normal and do not affect vision on their own.

What are medial Epicanthal folds?

Epicanthal folds are oblique or vertical folds from the upper or lower eyelids towards the medial canthus. Usually bilateral, they may involve either or both the upper and lower eyelids. These folds can be caused by excessive development of the skin across the bridge of the nose.

Is Epicanthal folds genetic?

The skin fold might cover part of the nasal sclera and, therefore, cause pseudoesotropia, that is, the eye appears to be crossed. The genetic basis for epicanthus is not well known, but is associated with several syndromes, including Down’s syndrome, Turner syndrome, and Zellweger syndrome.

What does Epicanthic fold look like?

Also know as an epicanthal fold, monolids are a piece of skin on the eyelid that runs from the nose to the eyebrow. It gives the eyelid the appearance of having no crease. 1 In some cases, it can make the eyelid more prominent and droopy, creating a more narrow appearance in the eye.

Do Epicanthic folds go away?

Epicanthus generally disappears by the age of puberty as the nasal bridge grows. Epicanthus inversus is usually seen in association with blepharophimosis and may be associated with relative shortage of skin in lateral periorbital area.

Is it normal for infants to have epicanthal folds?

Epicanthal folds may be normal for people of Asiatic descent and some non-Asian infants. Epicanthal folds also may be seen in young children of any race before the bridge of the nose begins to rise. However, they may also be due to certain medical conditions, including: Down syndrome. Fetal alcohol syndrome.

Where are the epicanthal folds on the face?

The fold runs from nose to the inner side of the eyebrow. Epicanthal folds may be normal for people of Asiatic descent and some non-Asian infants. Epicanthal folds also may be seen in young children of any race before the bridge of the nose begins to rise.

What are the medical conditions that cause epicanthal folds?

Epicanthal folds – However, they may also be due to certain medical conditions, including 1 Down syndrome. 2 Fetal alcohol syndrome. 3 Turner syndrome. 4 Phenylketonuria (PKU). 5 Williams syndrome. 6 (more items)

Can a child with Down syndrome have epicanthal folds?

If a child has epicanthal folds, and you suspect that another medical condition might be present, you can discuss it with your health care provider. Babies with down syndrome have an extra full or partial piece of chromosome 21, this causes a variety of physical abnormalities.