Literature DB >> 11094243

Ocular colobomata.

B C Onwochei1, J W Simon, J B Bateman, K C Couture, E Mir.   

Abstract

Ocular colobomata present diagnostic and therapeutic challenges in patients of all ages, but especially in young children. The "typical" coloboma, caused by defective closure of the fetal fissure, is located in the inferonasal quadrant, and it may affect any part of the globe traversed by the fissure from the iris to the optic nerve. Ocular colobomata are often associated with microphthalmia, and they may be idiopathic or associated with various syndromes. Types and severity of complications vary depending on the location and size of the colobomata. This article reviews the pathogeneses, categorization, genetic bases, differential diagnoses and management of ocular coloboma.

Entities:  

Mesh:

Year:  2000        PMID: 11094243     DOI: 10.1016/s0039-6257(00)00151-x

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  61 in total

Review 1.  Molecular mechanisms of optic vesicle development: complexities, ambiguities and controversies.

Authors:  Ruben Adler; M Valeria Canto-Soler
Journal:  Dev Biol       Date:  2007-02-07       Impact factor: 3.582

2.  The hyaloid vasculature facilitates basement membrane breakdown during choroid fissure closure in the zebrafish eye.

Authors:  Andrea James; Chanjae Lee; Andre M Williams; Krista Angileri; Kira L Lathrop; Jeffrey M Gross
Journal:  Dev Biol       Date:  2016-09-12       Impact factor: 3.582

Review 3.  Ocular coloboma: a reassessment in the age of molecular neuroscience.

Authors:  C Y Gregory-Evans; M J Williams; S Halford; K Gregory-Evans
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

4.  Visualization of the optic fissure in short-wavelength autofluorescence images of the fundus.

Authors:  Tobias Duncker; Jonathan P Greenberg; Janet R Sparrow; R Theodore Smith; Harry A Quigley; François C Delori
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-09-28       Impact factor: 4.799

5.  Two cases of CHARGE syndrome with multiple congenital anomalies.

Authors:  Joo Hyun Chang; Dong Ho Park; Jae Pil Shin; In Taek Kim
Journal:  Int Ophthalmol       Date:  2013-06-27       Impact factor: 2.031

6.  Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development.

Authors:  Nadean L Brown; Susan L Dagenais; Chuan-Min Chen; Tom Glaser
Journal:  Mamm Genome       Date:  2002-02       Impact factor: 2.957

7.  Triple Fundal Coloboma: irregular closure of the embryonic cleft in the optic cup.

Authors:  Ravi Bypareddy; Brijesh Takkar; Shorya Vardhan Azad; Rohan Chawla
Journal:  BMJ Case Rep       Date:  2016-09-27

8.  Oculocutaneous albinism with iridofundal coloboma.

Authors:  Gunjan Saluja; Shorya Vardhan Azad; Amar Pujari; Shreyas Temkar
Journal:  BMJ Case Rep       Date:  2018-01-26

9.  Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease.

Authors:  Christopher M Chou; Christine Nelson; Susan A Tarlé; Jonathan T Pribila; Tanya Bardakjian; Sean Woods; Adele Schneider; Tom Glaser
Journal:  Cell       Date:  2015-04-23       Impact factor: 41.582

10.  Iris coloboma in one eye and pigment dispersion syndrome in the fellow eye.

Authors:  Virgilio Galvis; Alejandro Tello; Paul Valarezo; Angélica M Prada
Journal:  BMJ Case Rep       Date:  2013-05-22
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