Literature DB >> 16352480

Bilateral complete isolated cryptophthalmos: a case report.

Deena Egier1, Robert Orton, Larry Allen, Victoria Mok Siu.   

Abstract

Cryptophthalmos is a condition of congenital eyelid malformation most commonly accompanied by syndactyly, urogenital anomalies, and cognitive impairments as in Fraser syndrome. We report on a patient with characteristic features consistent with autosomal dominant bilateral complete isolated cryptophthalmos. This patient represents only the sixth documented case of bilateral complete isolated cryptophthalmos. Defining characteristics of this variety are discussed, including bilateral central dimpling over the globes, normal eyebrow growth, and the absence of cognitive impairment. We introduce phenotypic features that distinguish bilateral isolated cryptophthalmos from other forms and discuss its relatively favorable prognosis.

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Year:  2005        PMID: 16352480     DOI: 10.1080/13816810500374557

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  2 in total

1.  A homozygous mutation p.Arg2167Trp in FREM2 causes isolated cryptophthalmos.

Authors:  Qian Yu; Bingying Lin; Shangqian Xie; Song Gao; Wei Li; Yizhi Liu; Hongwei Wang; Danping Huang; Zhi Xie
Journal:  Hum Mol Genet       Date:  2018-07-01       Impact factor: 6.150

Review 2.  Congenital upper eyelid coloboma: embryologic, nomenclatorial, nosologic, etiologic, pathogenetic, epidemiologic, clinical, and management perspectives.

Authors:  Hatem A Tawfik; Mohamed H Abdulhafez; Yousef A Fouad
Journal:  Ophthalmic Plast Reconstr Surg       Date:  2015 Jan-Feb       Impact factor: 1.746

  2 in total

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