Literature DB >> 12686301

The morphology and natural history of childhood cataracts.

Luis Amaya1, David Taylor, Isabelle Russell-Eggitt, Ken K Nischal, Dora Lengyel.   

Abstract

The morphology of congenital cataract reflects a combination of the timing and nature of the cause, the anatomy of the lens including its capsule, its development, and changes that take place with time. Morphology may variably affect prognosis, give a clue to the etiology and the age of onset and, in an isolated case, sometimes suggest heritability. The spectrum of morphological variations is enormous and can be complex. A comprehensive approach is to classify the variations according to the area of the lens involved, and sub-dividing them by a detailed description of the shape and appearance. Each specific morphological type is then analyzed determining the etiology, visual prognosis, and management. The use of gene markers has allowed many of these variations to be identified and categorized. Cataracts in childhood can involve the whole lens, in which case they are called total, Morgagnian, or disk-like. They can affect only the center of the lens: lamellar, nuclear, oil droplet, cortical, or coronary. They can be anterior: anterior polar, anterior subcapsular, or anterior lenticonus. The posterior aspect of the lens can also be affected in different fashions: Mittendorf's dot, posterior lenticonus, posterior cortical cataracts, or posterior subcapsular. There are five more forms that must be described separately: punctuate lens opacities, sutural cataracts, coralliform or crystalline, wedge-shaped, and persistent hyperplastic primary vitreous.

Entities:  

Mesh:

Year:  2003        PMID: 12686301     DOI: 10.1016/s0039-6257(02)00462-9

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


  51 in total

1.  Persistent central posterior capsule bulging after cataract extraction for posterior lenticonus.

Authors:  G D Kymionis; G A Kontadakis; A Plaka; I G Pallikaris
Journal:  Eye (Lond)       Date:  2012-03-02       Impact factor: 3.775

Review 2.  Molecular Genetics of Cataract.

Authors:  Alan Shiels; J Fielding Hejtmancik
Journal:  Prog Mol Biol Transl Sci       Date:  2015-06-12       Impact factor: 3.622

3.  Detection of c.139G>A (D47N) mutation in GJA8 gene in an extended family with inheritance of autosomal dominant zonular cataract without pulverulent opacities by exome sequencing.

Authors:  Padma Gunda; Mamata Manne; Syed Saifuddin Adeel; Ravi Kumar Reddy Kondareddy; Padma Tirunilai
Journal:  J Genet       Date:  2018-09       Impact factor: 1.166

4.  Intraocular lens implantation in pediatric eyes with posterior lentiglobus.

Authors:  M Edward Wilson; Rupal H Trivedi
Journal:  Trans Am Ophthalmol Soc       Date:  2006

5.  A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.

Authors:  Li-Yun Zhang; Bo Gong; Jian-Ping Tong; Dorothy Shu-Ping Fan; Sylvia Wai-Yee Chiang; Dinghua Lou; Dennis Shun-Chiu Lam; Gary Hin-Fai Yam; Chi-Pui Pang
Journal:  Mol Vis       Date:  2009-08-06       Impact factor: 2.367

6.  A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family.

Authors:  Wei Wang; Jin Jiang; Yanan Zhu; Jinyu Li; Chongfei Jin; Xingchao Shentu; Ke Yao
Journal:  Mol Vis       Date:  2010-03-25       Impact factor: 2.367

7.  A new locus for autosomal dominant congenital coronary cataract in a Chinese family maps to chromosome 3q.

Authors:  Guishun Liu; Yunbo Li; Yanfei Ruan; Wenping Cao; Li Xin; Jiangyuan Qian; Jingzhi Gu
Journal:  Mol Vis       Date:  2010-05-19       Impact factor: 2.367

Review 8.  Cat-Map: putting cataract on the map.

Authors:  Alan Shiels; Thomas M Bennett; J Fielding Hejtmancik
Journal:  Mol Vis       Date:  2010-10-08       Impact factor: 2.367

9.  Identification of a MIP mutation that activates a cryptic acceptor splice site in the 3' untranslated region.

Authors:  Chongfei Jin; Jin Jiang; Wei Wang; Ke Yao
Journal:  Mol Vis       Date:  2010-11-02       Impact factor: 2.367

10.  A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family.

Authors:  Kaijie Wang; Binbin Wang; Jing Wang; Shiyi Zhou; Bo Yun; Peisu Suo; Jie Cheng; Xu Ma; Siquan Zhu
Journal:  Mol Vis       Date:  2009-12-16       Impact factor: 2.367

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