Literature DB >> 3079999

Peters' anomaly as a consequence of genetic and nongenetic syndromes.

J D Kivlin, R M Fineman, A S Crandall, R J Olson.   

Abstract

A new syndrome includes Peters' anomaly and short-limbed dwarfism. A balanced chromosomal translocation in the brother (patient 1) appears to be coincidental to the physical abnormalities, because his sister (patient 2) has identical findings but normal fibroblast and lymphocyte karyotypes. Peters' anomaly, which includes corneal clouding, iris and/or lens adhesions to the cornea, and the absence of endothelium and Descemet's membrane, is often associated with systemic abnormalities. Since there are different genetic and nongenetic systemic conditions that include Peters' anomaly, and there are several ocular syndromes with features overlapping this disorder, we believe that Peters' anomaly is a morphologic finding rather than a distinct entity.

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Mesh:

Year:  1986        PMID: 3079999     DOI: 10.1001/archopht.1986.01050130071022

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  8 in total

1.  Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance.

Authors:  J C de Almeida; D F Reis; J Llerena Júnior; J Barbosa Neto; R L Pontes; S Middleton; L F Telles
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

Review 2.  Glaucoma genetics.

Authors:  Pratap Challa
Journal:  Int Ophthalmol Clin       Date:  2008

3.  Transplantation of congenitally opaque corneas.

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

4.  Heterogeneity in dominant anterior segment malformations.

Authors:  G E Holmström; W P Reardon; M Baraitser; J S Elston; D S Taylor
Journal:  Br J Ophthalmol       Date:  1991-10       Impact factor: 4.638

5.  Glaucoma and Peters' anomaly. A clinicopathologic case report.

Authors:  D H Heath; M B Shields
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

Review 6.  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

7.  Peters plus syndrome and absence of kidney: a case report.

Authors:  Navneet Tuli; Suresh Kumar; Sunandan Sood
Journal:  Cases J       Date:  2009-01-01

8.  Anterior segment dysgenesis after overexpression of transforming growth factor-beta-induced gene, beta igh3, in the mouse eye.

Authors:  Jung-Eun Kim; Min-Su Han; Yong-Chul Bae; Hong-Kyun Kim; Tae-Im Kim; Eung Kweon Kim; In-San Kim
Journal:  Mol Vis       Date:  2007-10-16       Impact factor: 2.367

  8 in total

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