Literature DB >> 11095131

Microblepharon: a case report.

D R Jordan1, I P Hwang, R Pashby.   

Abstract

Microblepharon is a rare congenital anomaly manifested by a vertical shortening of the eyelids. We describe the clinical presentation and surgical outcome of a patient with trisomy 21 and microblepharon. Microblepharon occurs in varying degrees and must be distinguished from ablepharon and cryptophthalmos. A variety of surgical options are available depending upon the degree of lid involvement.

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Year:  2000        PMID: 11095131

Source DB:  PubMed          Journal:  Ophthalmic Surg Lasers        ISSN: 1082-3069


  2 in total

1.  Isolated severe microblepharon in a neonate: a rare case.

Authors:  Rachna Meel; Saranya Devi; Anita Ganger; Manasa S; Neelam Pushker
Journal:  Int Ophthalmol       Date:  2017-08-12       Impact factor: 2.031

Review 2.  Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.

Authors:  A M Slavotinek; C J Tifft
Journal:  J Med Genet       Date:  2002-09       Impact factor: 6.318

  2 in total

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