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Ophthalmic Paediatrics and Genetics Volume 13, 1992 - Issue 2
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Original Article

The Spectrum of Associated Ocular and Systemic Malformations

Elise Heon Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada; Department of Genetics, Hospital for Sick Children, University of Toronto, Toronto, Ont, Canada
,
Magda Barsoum-Homsy Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada
,
Line Cevrette Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada
,
Jean-Louis Jacob Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada
,
Jean Milot Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada
,
Robert Polemeno Department of Ophthalmology, University of Montreal, Hôpital Ste-Justine, Montreal, Que, Canada
&
Maria A. Musarella Department of Ophthalmology, Hospital for Sick Children, University of Toronto, Toronto, Ont, Canada; Departments of Ophthalmology and Genetics, Hospital for Sick Children, Toronto, Ont, Canada
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Pages 137-143 | Accepted 09 Mar 1992, Published online: 08 Jul 2009

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Raksheeth Nathan Rajagopal & Merle Fernandes. (2023) Peters Anomaly: Novel Non-Invasive Alternatives to Penetrating Keratoplasty. Seminars in Ophthalmology 38:3, pages 275-282.
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K. Aliferis, C. Marsal, V. Pelletier, B. Doray, M.M. Weiss, C.M.J. Tops, C. Speeg-Schatz, S.A.J. Lesnik & H. Dollfus. (2010) A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly. Ophthalmic Genetics 31:4, pages 205-208.
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Deepak Edward, Ali Al Rajhi, Richard Alan Lewis, Stacey Curry, Zongren Wang & Bassem Bejjani. (2004) Molecular basis of Peters anomaly in Saudi Arabia. Ophthalmic Genetics 25:4, pages 257-270.
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Werner Götz. (1995) Transgenic models for eye malformations. Ophthalmic Genetics 16:3, pages 85-104.
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Articles from other publishers (31)

Uri Elbaz, Asim Ali, Hermina Strungaru & Kamiar Mireskandari. (2022) Phenotypic Spectrum of Peters Anomaly: Implications for Management. Cornea 41:2, pages 192-200.
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Helen H. Yeung, Allison Loh & David S. Walton. 2022. Albert and Jakobiec's Principles and Practice of Ophthalmology. Albert and Jakobiec's Principles and Practice of Ophthalmology 6653 6671 .
Ye Elaine Wang, Dhariana Acon Ramirez, Ta Chen Chang & Audina Berrocal. (2020) Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report. BMC Ophthalmology 20:1.
Crossref
Helen H. Yeung, Allison Loh & David S. Walton. 2020. Albert and Jakobiec's Principles and Practice of Ophthalmology. Albert and Jakobiec's Principles and Practice of Ophthalmology 1 19 .
SudarshanKumar Khokhar, Ganesh Pillay, Chirakshi Dhull, Esha Agarwal, Manish Mahabir & Pulak Aggarwal. (2017) Pediatric cataract. Indian Journal of Ophthalmology 65:12, pages 1340.
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Hannah Happ, Kala F. Schilter, Eric Weh, Linda M. Reis & Elena V. Semina. (2016) 8q21.11 microdeletion in two patients with syndromic peters anomaly. American Journal of Medical Genetics Part A 170:9, pages 2471-2475.
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Shahid Y. Khan, Shivakumar Vasanth, Firoz Kabir, John D. Gottsch, Arif O. Khan, Raghothama Chaerkady, Mei-Chong W. Lee, Carmen C. Leitch, Zhiwei Ma, Julie Laux, Rafael Villasmil, Shaheen N. Khan, Sheikh Riazuddin, Javed Akram, Robert N. Cole, C. Conover Talbot, Nader Pourmand, Norann A. Zaghloul, J. Fielding Hejtmancik & S. Amer Riazuddin. (2016) FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1. Nature Communications 7:1.
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Darshan Kumar U. Kansara & Sunil G. Biradar. (2015) PETER’S TYPE II ANOMALY ASSOCIATED WITH CONGENITAL HEART DEFECT: RARE CASE REPORT. Journal of Evidence Based Medicine and Healthcare 2:10, pages 1565-1568.
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Anagha Medsinge & Ken K. Nischal. (2015) Cataract surgery in children with congenital keratolenticular adhesion (Peters anomaly type 2). Journal of American Association for Pediatric Ophthalmology and Strabismus 19:1, pages 24-28.
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Tero Kivelä, Elisabeth M. Messmer & Beata Rymgayłło-Jankowska. 2015. Eye Pathology. Eye Pathology 79 154 .
E. Weh, L.M. Reis, R.C. Tyler, D. Bick, W.J. Rhead, S. Wallace, T.L. McGregor, S.K. Dills, M.-C. Chao, J.C. Murray & E.V. Semina. (2014) Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes . Clinical Genetics 86:2, pages 142-148.
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Anuradha Ganesh, Dang Tam Mai & Alex V. Levin. (2013) Pediatric glaucoma terminology. American Journal of Medical Genetics Part A 161:12, pages 3205-3215.
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Kristin M. Hammersmith, Renata A. Rezende, Elisabeth J. Cohen, Ralph C. EagleJrJr & Christopher J. Rapuano. 2011. Cornea. Cornea 239 265 .
Osamu Motoyama, Hiroko Arai, Ryoko Harada, Kei Hasegawa & Kikuo Iitaka. (2010) A girl with Peters plus syndrome associated with myelomeningocele and chronic renal failure. Clinical and Experimental Nephrology 14:4, pages 381-384.
Crossref
Joel Sugar & Hormuz P. Wadia. 2009. Ophthalmology. Ophthalmology 214 218 .
Robert L Stamper, Marc F Lieberman & Michael V Drake. 2009. Becker-Shaffer's Diagnosis and Therapy of the Glaucomas. Becker-Shaffer's Diagnosis and Therapy of the Glaucomas 294 329 .
Linda M. Reis, Rebecca C. Tyler, Omar Abdul‐Rahman, Pamela Trapane, Robert Wallerstein, Diane Broome, Jodi Hoffman, Aneal Khan, Christina Paradiso, Nitin Ron, Amanda Bergner & Elena V. Semina. (2008) Mutation analysis of B3GALTL in Peters Plus syndrome . American Journal of Medical Genetics Part A 146A:20, pages 2603-2610.
Crossref
Murat Kadri Erdoğan, Gülen Eda Utine, Yasemin Alanay & Dilek Aktaş. (2008) Unilateral Petersʼ anomaly in an infant with 22q11.2 deletion syndrome. Clinical Dysmorphology 17:4, pages 289-290.
Crossref
Esther Kinning & Margaret Barrow. (2008) Arthrogryposis in association with Peters' anomaly. Clinical Dysmorphology 17:3, pages 177-179.
Crossref
Karina Nagao & David S. Walton. 2008. Albert &amp Jakobiec's Principles &amp Practice of Ophthalmology. Albert &amp Jakobiec's Principles &amp Practice of Ophthalmology 4201 4212 .
Dany M. Najjar, Stephen P. Christiansen, Erick D. Bothun & C. Gail Summers. (2006) Strabismus and Amblyopia in Bilateral Peters Anomaly. Journal of American Association for Pediatric Ophthalmology and Strabismus 10:3, pages 193-197.
Crossref
P. Dureau. (2006) Glaucomes congénitaux et trabéculodysgénésies : aspects cliniques et génétiques. Journal Français d'Ophtalmologie 29:2, pages 198-215.
Crossref
F. Hampton Roy. (2005) Pseudo-developmental glaucoma. Annals of Ophthalmology 37:4, pages 245-251.
Crossref
Mayumi Morimoto, Tomoyuki Takano, Yuko Sakaue, Chihiro Sawai, Hirofumi Aotani, Shigeki Koshida & Yoshihiro Takeuchi. (2004) Peters' anomaly with bilateral perisylvian polymicrogyria and abdominal calcification. Congenital Anomalies 44:2, pages 99-102.
Crossref
Ian M MacDonald, Mai Tran & Maria A Musarella. (2004) Ocular genetics: current understanding. Survey of Ophthalmology 49:2, pages 159-196.
Crossref
Lucy L.H Yang, Scott R Lambert, Michael J Lynn & R.Doyle Stulting. (2004) Surgical management of glaucoma in infants and children with Peters' anomaly. Ophthalmology 111:1, pages 112-117.
Crossref
Liesbeth J.J.M. Maillette de Buy Wenniger-Prick & Raoul C.M. Hennekam. (2002) The Peters’ plus syndrome: a review. Annales de Génétique 45:2, pages 97-103.
Crossref
Stephen J Withers, Glen A Gole & Kim M Summers. (2001) Autosomal dominant cataracts and Peters anomaly in a large Australian family. Clinical Genetics 55:4, pages 240-247.
Crossref
U. Moog, E.M. Bleeker-Wagemakers, P. Crobach, J.S.H. Vles & C.T.R.M. Schrander-Stumpel. (1998) Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: A new autosomal recessive syndrome?. American Journal of Medical Genetics 78:3, pages 263-266.
Crossref
Bruce A Miller & Zane F Pollard. (1995) Case Report: Two Eyes in One Patient Representing the Spectrum of Peter's Anomaly. Journal of Pediatric Ophthalmology & Strabismus 32:6, pages 388-389.
Crossref
Isabel M. Hanson, Judy M. Fletcher, Tim Jordan, Alison Brown, David Taylor, Rebecca J. Adams, Hope H. Punnett & Veronica van Heyningen. (1994) Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly. Nature Genetics 6:2, pages 168-173.
Crossref

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