Literature DB >> 808872

Anterior chamber cleavage syndrome. A stepladder classification.

G O Waring, M M Rodrigues, P R Laibson.   

Abstract

This paper classifies the abnormalities of the anterior chamber cleavage syndrome (mesodermal dysgenesis of the iris and cornea). The anatomic findings are arranged in a tabular stepladder fashion which builds from simple to more complex combinations, most of which have been previously known by eponyms. There are three groups of anomalies: 1) peripheral, 2) central, and 3) combinations of the two. 1) The peripheral anomalies consist of a prominent Schwalbe's ring, iris strands to Schwalbe's ring, and hypoplasia of the anterior iris stroma. Developmental glaucoma is commonly present. 2) The essential feature of the central anomalies is a defect in the corneal endothelium and Descemet's membrane with an overlying corneal opacity. Additional components include central iridocorneal adhesions, keratolenticular approximation with cataract, and scleralizaiton of the cornea. Chorioretinal anomalies, developmental glaucoma, and systemic malformations may be present. 3) Central and peripheral combinations may exist in the same eye, in both eyes of the same patient, or within the same family.

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Year:  1975        PMID: 808872     DOI: 10.1016/0039-6257(75)90034-x

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  37 in total

1.  Alagille syndrome: family studies.

Authors:  F V Elmslie; A J Vivian; H Gardiner; C Hall; A P Mowat; R M Winter
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

Review 2.  Genetics of aniridia and anterior segment dysgenesis.

Authors:  A Churchill; A Booth
Journal:  Br J Ophthalmol       Date:  1996-07       Impact factor: 4.638

Review 3.  Alagille syndrome.

Authors:  I D Krantz; D A Piccoli; N B Spinner
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

4.  Monoclonal antibody to the corneal endothelium: partial characterization of the antigen and its expression in fetal and adult rabbits.

Authors:  T Sakamoto; Y Nakashima; K Maeda; K Sueishi
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

5.  Congenital ocular and other systemic abnormalities associated with ring-11 chromosome.

Authors:  S Daniele; F Pecorelli; L Tiepolo; R Armellini; F S Liotti
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1986       Impact factor: 3.117

6.  Warburg (HARD +/- E) syndrome without retinal dysplasia: case report and review.

Authors:  M F Attia; J Burn; J H McCarthy; D P Purohit; D W Milligan
Journal:  Br J Ophthalmol       Date:  1986-10       Impact factor: 4.638

7.  [Histological findings in dysgenesis mesodermalis iridis et corneae Rieger].

Authors:  R Troeber; R Rochels
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1980

8.  Fate mapping of neural crest cells during eye development using a protein 0 promoter-driven transgenic technique.

Authors:  Keiichiro Iwao; Masaru Inatani; Satoshi Okinami; Hidenobu Tanihara
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2008-05-06       Impact factor: 3.117

9.  Autosomal dominant iridogoniodysgenesis with associated somatic anomalies: four-generation family with Rieger's syndrome.

Authors:  I A Chisholm; A E Chudley
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638

10.  Evaluation of MFRP as a candidate gene for high hyperopia.

Authors:  Panfeng Wang; Zhikuan Yang; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-01-23       Impact factor: 2.367

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