Literature DB >> 20451863

Atypical Peters plus syndrome with new associations.

Nancy N Hanna1, Kimberly Eickholt, Dimitri Agamanolis, Robert Burnstine, Deepak P Edward.   

Abstract

Peters plus syndrome is a rare condition, with ocular and systemic malformations. We describe a case of unilateral Peters anomaly with previously unreported systemic findings associated with this syndrome. In addition, autopsy findings suggested that severe developmental angle anomalies may be the cause of glaucoma in some of these patients. Copyright 2010 American Association for Pediatric Ophthalmology and Strabismus. Published by Mosby, Inc. All rights reserved.

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Year:  2010        PMID: 20451863     DOI: 10.1016/j.jaapos.2010.02.003

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  5 in total

Review 1.  Genetics of anterior segment dysgenesis disorders.

Authors:  Linda M Reis; Elena V Semina
Journal:  Curr Opin Ophthalmol       Date:  2011-09       Impact factor: 3.761

Review 2.  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

3.  Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome.

Authors:  Eric Weh; Hideyuki Takeuchi; Sanaa Muheisen; Robert S Haltiwanger; Elena V Semina
Journal:  PLoS One       Date:  2017-09-19       Impact factor: 3.240

Review 4.  Genetic Syndromes Associated with Congenital Cardiac Defects and Ophthalmologic Changes - Systematization for Diagnosis in the Clinical Practice.

Authors:  Priscila H A Oliveira; Beatriz S Souza; Eimi N Pacheco; Michele S Menegazzo; Ivan S Corrêa; Paulo R G Zen; Rafael F M Rosa; Claudia C Cesa; Lucia C Pellanda; Manuel A P Vilela
Journal:  Arq Bras Cardiol       Date:  2018-01       Impact factor: 2.000

5.  An Unusual Case of Peters Plus Syndrome with Sexual Ambiguity and Absence of Mutations in the B3GALTL Gene.

Authors:  Olfa Siala; Neila Belguith; Faiza Fakhfakh
Journal:  Iran J Pediatr       Date:  2013-08       Impact factor: 0.364

  5 in total

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