Localised unilateral blepharochalasis.

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Localised unilateral blepharochalasis.

In 1807 Beers' described a condition which was later named blepharochalasis (Gk=eyelid slackening) by Fuchs.2 The condition consists of recurrent attacks of oedema of the eyelids and in chronic conditions the skin becomes reddish, thin, and redundant. Periorbital sequelae include ptosis, pseudoepicanthic fold with underlying nasal fat pad atrophy, blepharophimosis, proptosis, lower lid malposit...

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Blepharochalasis.

Blepharochalasis is an uncommon disorder distinguished by recurrent episodes of eyelid oedema in young patients. A hypertrophic form, manifested as fat herniation, and an atrophic form, manifested as fat atrophy, have been described. Ptosis with excellent levator function, laxity of the lateral canthal structures with rounding of the lateral canthal angle, nasal fat pad atrophy, and redundant e...

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Unilateral and segmental localised polycystic kidney disease.

Unilateral and segmental localised polycystic disease is a rare type of cystic disease of the kidney. It takes the form of a segmental cystic abnormality in one kidney morphologically identical to the autosomal dominant adult form of polycystic kidney disease. The clinical, radiological, and pathological appearances of a case are described. The differential diagnosis and a possible pathogenic m...

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Blepharochalasis with multiple system involvement.

A rare case of bilateral blepharochalasis of the upper eyelids is presented in a 10-year-old boy with several systemic abnormalities--unilateral agenesis of the left kidney, multiple skeletal anomalies of the vertebral column, and congenital heart disease with a left to right shunt. Such widespread congenital defects in association with blepharochalasis have not been described before. Blepharoc...

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An Unusual Case of Blepharochalasis

PURPOSE To describe a rare case of blepharochalasis that progressed from unilateral to bilateral involvement at five years after disease onset. CASE REPORT A previously healthy five-year-old white boy presented to our hospital for a screening visual examination. He was found to have a 2-mm right eyelid ptosis with crepe-like skin and subcutaneous telangiectatic vessels. His mother noted that ...

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ژورنال

عنوان ژورنال: British Journal of Ophthalmology

سال: 1994

ISSN: 0007-1161

DOI: 10.1136/bjo.78.11.881