Results 171 to 180 of about 3,419 (204)
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One-Stage Repair of Blepharophimosis
Plastic and Reconstructive Surgery, 1991Congenital blepharophimosis is a congenital anomaly characterized by abnormalities in the area of the eyes, including bilateral ptosis, shortening of the horizontal fissure of the lid, expansion of the intercanthal distance, and epicanthus inversus.
T, Nakajima +3 more
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Blepharophimosis and Cardiopathy
Journal of Pediatric Ophthalmology & Strabismus, 1980A 2 1/2-year-old girl with blepharophimosis and ventriculoseptal defect is described. Blepharophimosis is rare, and this complex more so. Yet, the clinical implications of its recognition are potentially important.
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Blepharophimosis Syndrome With Absent Tear Production
Ophthalmic Plastic & Reconstructive Surgery, 2015The purpose of this report was to present a case of congenital alacrima in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES). A 9-month-old boy presented with characteristic clinical findings of BPES confirmed by genetic testing. On further history taking and evaluation, the patient was noted to have no tear production, despite
Jacqueline K, Ng +3 more
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The Five-Flap Technique for Blepharophimosis
Archives of Ophthalmology, 1989The correction of epicanthus associated with blepharophimosis is a difficult surgical problem. Most commonly used techniques, such as the Mustardé technique, require meticulous measurements, and their theoretical geometric basis and flap designs are often confusing.
R L, Anderson, T S, Nowinski
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Blepharophimosis–ptosis–epicanthus inversus syndrome (BPES)
International Journal of Dermatology, 2007Blepharophimosis–ptosis–epicanthus inversus syndrome (BPES) is a rare inherited condition that includes characteristic eyelid malformations and sometimes reduced fertility in females. Genetic studies have implicated mutations in the forkhead transcription factor FOXL2 as responsible for BPES.We report a female and her father with BPES type I, who ...
Alvaro, Leon-Mateos +4 more
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Blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES)
Acta Ophthalmologica Scandinavica, 1996ABSTRACT The blepharophimosis‐ptosis‐epicanthus inversus syndrome is characterized by shortening of the horizontal orbital fissure (blepharophimosis), congenital ptosis and epicanthus inversus. The condition may occur either as an autosomal dominant trait (blepharophimosis‐ptosis‐epicanthus inversus syndrome types 1 and 2), or sporadically ...
P, Strømme, F, Sandboe
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Ptosis with blepharophimosis and epicanthus inversus
British Journal of Plastic Surgery, 1986The rare syndrome which includes ptosis, blepharophimosis and epicanthus inversus is recorded in one family through five generations. The genetic significance of the syndrome is emphasised and the literature on the surgical management of the condition reviewed.
D, Elliot, A F, Wallace
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Blepharophimosis with Associated Cup-Lop Ears
Annals of Plastic Surgery, 1978Blepharophimosis is a rare congenital triad consisting of epicanthus inversus, blepharoptosis, and a wider than normal intercanthal distance. Attention has recently been drawn to abnormalities of the eyebrow and the poorly developed nasal bridge. I record 9 cases of blepharophimosis associated with cup-lop ears seen over the last 15 years.
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Dominantly inherited syndromic blepharophimosis
American Journal of Medical Genetics, 1989Cette breve analyse inventorie rapidement les manifestations de ce syndrome, manifestations oculaires et retro-oculaires (division palatine, syndactylie, hernie inguinale).
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One-Stage Repair of Blepharophimosis
Plastic and Reconstructive Surgery, 1994Blepharophimosis is a congenital malformation involving the orbital region. It is associated with ptosis of the upper eyelids, epicanthal folds, telecanthus, and flattened and widened nasal bridge. We have surgically treated five cases of blepharophimosis by a procedure in which nasal bone graft, medial canthoplasty, and fascial suspension are ...
Karacaoglan, N +3 more
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