Blepharophimosis is a rare congenital disorder characterized by a narrow opening of the eyes and drooping eyelids. It affects the upper eyelids, causing them to appear smaller than usual. This condition can affect one or both eyes and can be part of a genetic syndrome, such as Blepharophimosis Syndrome (BPES).
The right upper eyelid may be affected more severely than the left, leading to asymmetry. The narrowing of the opening of the eye can also cause difficulty with vision, particularly in severe cases.
Symptoms of blepharophimosis right upper eyelid include:
Blepharophimosis can be caused by mutations in the FOXL2 gene and is inherited in an autosomal dominant pattern. It can also occur as a result of a spontaneous genetic mutation.
Other conditions may also cause similar symptoms, such as ptosis, which is a drooping of the eyelid due to weakened muscles, or congenital ectropion, which is an outward turning of the eyelid.
A proper diagnosis of blepharophimosis right upper eyelid is important to rule out other conditions and to determine the appropriate treatment plan. This may include genetic testing to identify any underlying genetic mutations or other diagnostic tests such as a visual field test.
Blepharophimosis right upper eyelid is a rare congenital disorder that affects the upper eyelids, causing a narrowing of the opening of the eyes and drooping of the eyelids. It can be part of a genetic syndrome and is caused by mutations in the FOXL2 gene. A proper diagnosis is important to determine the appropriate treatment plan and to rule out other conditions with similar symptoms.
Blepharophimosis is a rare genetic condition that affects the eyelids, causing them to droop and narrow. The condition can affect both eyes, but it is more commonly seen in the upper eyelids. This condition can cause vision problems, and it can also affect the appearance of the eyes.
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