Literature DB >> 1495764

Peters' anomaly. The spectrum of associated ocular and systemic malformations.

E Heon1, M Barsoum-Homsy, L Cevrette, J L Jacob, J Milot, R Polemeno, M A Musarella.   

Abstract

The cases of Peters' anomaly seen over the past decade, at Hospital Ste-Justine in Montreal, are reviewed. Associated ocular anomalies were observed in 50% of cases while 60% of patients presented with associated systemic defects. It is clear, from these patients and those reported in the literature, that Peters' anomaly can be an isolated condition, or part of distinct syndromes: the Krause-Kivlin syndrome or the Peters'-plus syndrome. The authors emphasize the importance for the ophthalmologist to recognize these possibilities if proper management is to be provided.

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Year:  1992        PMID: 1495764     DOI: 10.3109/13816819209087614

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  12 in total

1.  Histopathological examination of two cases of anterior staphyloma associated with Peters' anomaly and persistent hyperplastic primary vitreous.

Authors:  A Matsubara; H Ozeki; N Matsunaga; M Nozaki; M Ashikari; S Shirai; Y Ogura
Journal:  Br J Ophthalmol       Date:  2001-12       Impact factor: 4.638

2.  Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes.

Authors:  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
Journal:  Clin Genet       Date:  2013-09-17       Impact factor: 4.438

3.  Mutation analysis of B3GALTL in Peters Plus syndrome.

Authors:  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
Journal:  Am J Med Genet A       Date:  2008-10-15       Impact factor: 2.802

4.  A girl with Peters plus syndrome associated with myelomeningocele and chronic renal failure.

Authors:  Osamu Motoyama; Hiroko Arai; Ryoko Harada; Kei Hasegawa; Kikuo Iitaka
Journal:  Clin Exp Nephrol       Date:  2010-04-28       Impact factor: 2.801

5.  Transplantation of congenitally opaque corneas.

Authors:  B E Frueh; S I Brown
Journal:  Br J Ophthalmol       Date:  1997-12       Impact factor: 4.638

Review 6.  8q21.11 microdeletion in two patients with syndromic peters anomaly.

Authors:  Hannah Happ; Kala F Schilter; Eric Weh; Linda M Reis; Elena V Semina
Journal:  Am J Med Genet A       Date:  2016-07-05       Impact factor: 2.802

Review 7.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367

8.  Analysis of FOXD3 sequence variation in human ocular disease.

Authors:  Bethany A Volkmann Kloss; Linda M Reis; Dominique Brémond-Gignac; Tom Glaser; Elena V Semina
Journal:  Mol Vis       Date:  2012-06-27       Impact factor: 2.367

9.  Congenital corneal staphyloma.

Authors:  Hossein Salour; Nasser Owji; Alireza Sadeghipour
Journal:  J Ophthalmic Vis Res       Date:  2009-07

10.  FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.

Authors:  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
Journal:  Nat Commun       Date:  2016-04-06       Impact factor: 14.919

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