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Blepharochalasis is an inflammation of the eyelid that is characterized by exacerbations and remissions of eyelid edema, which results in a stretching and subsequent atrophy of the eyelid tissue, leading to the formation of redundant folds over the lid margins. It typically affects only the upper eyelids, and may be unilateral as well as bilateral.
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Ascher's syndrome is a rare clinical entity distinguished by blepharochalasis, double upper lip appearance, and nontoxic goiter. Nontoxic goiter is a rare finding, occurring in only 10-50% of cases. It may appear several years following the onset of blepharochalasis, so it is not
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Blepharitis is characterized by chronic inflammation of the eyelid, usually at the base of the eyelashes. [3] [4] [5] Symptoms include inflammation, irritation, itchiness, a burning sensation, excessive tearing, and crusting and sticking of eyelids.
The elderly version may begin to develop as early as 40 years of age, and it continues to progress with age. [2] The congenital version may begin around 20 years of age. [ 2 ] There is no racial predisposition towards developing dermatochalasis, and men and women are equally affected.
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Brown syndrome can be divided in two categories based on the restriction of movement on the eye itself and how it affects the eye excluding the movement: [3] Congenital (present at birth) Brown syndrome results from structural anomalies other than a short tendon sheath but other fibrous adhesions may be present around the trochlear area.
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