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Original Article

Congenital cataract with microcornea and Peters’ anomaly as expressions of one autosomal dominant gene

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Pages 187-194 | Published online: 08 Jul 2009

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Ursula M. Mayer. (1992) Peters' Anomaly and Combination with Other Malformations (Series of 16 Patients). Ophthalmic Paediatrics and Genetics 13:2, pages 131-135.
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Cynthia S. Cook. (1989) Experimental models of anterior segment dysgenesis. Ophthalmic Paediatrics and Genetics 10:1, pages 33-46.
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Articles from other publishers (20)

Lance Doucette, Jane Green, Bridget Fernandez, Gordon J Johnson, Patrick Parfrey & Terry-Lynn Young. (2010) A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly. European Journal of Human Genetics 19:3, pages 293-299.
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Nilufer Berker, Yasemin Alanay, Ufuk Elgin, Bilge Volkan-Salanci, Tulay Simsek, Nurten Akarsu & Mehmet Alikasifoglu. (2009) A new autosomal dominant Peters’ anomaly phenotype expanding the anterior segment dysgenesis spectrum. Acta Ophthalmologica 87:1, pages 52-57.
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Pratap Challa. (2008) Glaucoma Genetics. International Ophthalmology Clinics 48:4, pages 73-94.
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Natalya S Zinkevich, Dmitry V Bosenko, Brian A Link & Elena V Semina. (2006) laminin alpha 1gene is essential for normal lens development in zebrafish. BMC Developmental Biology 6:1.
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Elena V. Semina, Dmitry V. Bosenko, Natalya C. Zinkevich, Kelly A. Soules, David R. Hyde, Thomas S. Vihtelic, Gregory B. Willer, Ronald G. Gregg & Brian A. Link. (2006) Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish. Developmental Biology 299:1, pages 63-77.
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P. Dureau. (2006) Glaucomes congénitaux et trabéculodysgénésies : aspects cliniques et génétiques. Journal Français d'Ophtalmologie 29:2, pages 198-215.
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Saul Merin. 2005. Inherited Eye Diseases. Inherited Eye Diseases 125 166 .
Pratap Challa. (2004) Glaucoma Genetics: Advancing New Understandings of Glaucoma Pathogenesis. International Ophthalmology Clinics 44:2, pages 167-185.
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Ken K. Nischal. 2003. Pediatric Ophthalmology and Strabismus. Pediatric Ophthalmology and Strabismus 391 429 .
Albert S Jun, Karl W Broman, Diana V Do, Esen K Akpek, Walter J Stark & John D Gottsch. (2002) Endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning (edict) syndrome maps to chromosome 15q22.1?q25.3. American Journal of Ophthalmology 134:2, pages 172-176.
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Young Suk Yu, Jin Hak Lee & Bong Leen Chang. (2000) Surgical management of congenital cataract associated with severe microphthalmos. Journal of Cataract and Refractive Surgery 26:8, pages 1219-1224.
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Rosanna Pallotta, Paola Fusilli, Giuseppe Sabatino, Alberto Verrotti & Francesco Chiarelli. (1998) Confirmation of the colobomatous macrophthalmia with microcornea syndrome: Report of another family. American Journal of Medical Genetics 76:3, pages 252-254.
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B Seitz & G O Naumann. (1996) Bilateral congenital dentiform cataract and extreme microcornea in eyes with uveal colobomas and persistent hyperplastic primary vitreous.. British Journal of Ophthalmology 80:4, pages 378-379.
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Mark H. Scott, J. Fielding Hejtmancik, Laura A. Wozencraft, Leanne M. Reuter, Marshall M. Parks & Muriel I. Kaiser-Kupfer. (1994) Autosomal Dominant Congenital Cataract. Ophthalmology 101:5, pages 866-871.
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W Michael Myles, Michael E Flanders, David Chitayat & Seymour Brownstein. (1992) Peters' Anomaly: A Clinicopathologic Study. Journal of Pediatric Ophthalmology & Strabismus 29:6, pages 374-381.
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Ignacio R. Rodriguez, Pedro Gonzales, J. Samuel ZiglerJr.Jr. & Teresa Borrás. (1992) A guinea-pig hereditary cataract contains a splice-site deletion in a crystallin gene. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1180:1, pages 44-52.
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G. E. Holmstrom, W. P. Reardon, M. Baraitser, J. S. Elston & D. S. Taylor. (1991) Heterogeneity in dominant anterior segment malformations.. British Journal of Ophthalmology 75:10, pages 591-597.
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Fred S. Bodker, Mary Ann Lavery, Thomas N. Mitchell, Everett W. Lovrien & Irene H. Maumenee. (1990) Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts. American Journal of Medical Genetics 37:1, pages 54-59.
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Richard Alan Lewis, Robert L. Nussbaum & Dwight Stambolian. (1990) Mapping X-linked Ophthalmic Diseases. Ophthalmology 97:1, pages 110-121.
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Cynthia S Cook & Kathleen K Sulik. (1988) Keratolenticular Dysgenesis (Peters' Anomaly) as a Result of Acute Embryonic Insult During Gastrulation. Journal of Pediatric Ophthalmology & Strabismus 25:2, pages 60-66.
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