Literature DB >> 24138040

Genetics of ectopia lentis.

Mohammad Ali Sadiq1, Deborah Vanderveen.   

Abstract

Hereditary ectopia lentis or lens subluxation can occur with and without systemic associations. Significant overlap can be found in the genetic mutations and pathogenesis of subluxated lenses in their isolated forms as well as with associated syndromes. Gene mutations have been identified for lens subluxation associated with Marfan syndrome, Weill Marchesani syndrome, Ectopia Lentis simplex, Ectopia Lentis et pupillae, Ehlers Danlos syndrome, homocystinuria, and sulfite oxidase deficiency. Herein we describe the ocular and systemic characteristics found in patients with ectopia lentis, as well as the gene mutations identified thus far.

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Mesh:

Year:  2013        PMID: 24138040     DOI: 10.3109/08820538.2013.825276

Source DB:  PubMed          Journal:  Semin Ophthalmol        ISSN: 0882-0538            Impact factor:   1.975


  18 in total

1.  Human eye development is characterized by coordinated expression of fibrillin isoforms.

Authors:  Dirk Hubmacher; Dieter P Reinhardt; Thomas Plesec; Katja Schenke-Layland; Suneel S Apte
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-11-18       Impact factor: 4.799

Review 2.  ADAMTS proteins as modulators of microfibril formation and function.

Authors:  Dirk Hubmacher; Suneel S Apte
Journal:  Matrix Biol       Date:  2015-05-07       Impact factor: 11.583

3.  Next-generation sequencing panel analysis in 24 Chinese patients with congenital ectopia lentis.

Authors:  Meng Qi; Chong Wang; Yi Liu; Xiangyu Shi; WeiNing Rong
Journal:  Int Ophthalmol       Date:  2022-05-25       Impact factor: 2.029

4.  Anterior pituitary, sex hormones, and keratoconus: Beyond traditional targets.

Authors:  Dimitrios Karamichos; Paulina Escandon; Brenda Vasini; Sarah E Nicholas; Lyly Van; Deanna H Dang; Rebecca L Cunningham; Kamran M Riaz
Journal:  Prog Retin Eye Res       Date:  2021-11-02       Impact factor: 19.704

5.  Altered hepatic sulfur metabolism in cystathionine β-synthase-deficient homocystinuria: regulatory role of taurine on competing cysteine oxidation pathways.

Authors:  Hua Jiang; Sally P Stabler; Robert H Allen; Steven H Abman; Kenneth N Maclean
Journal:  FASEB J       Date:  2014-06-02       Impact factor: 5.191

6.  Scleral-Fixated Intraocular Lenses: Past and Present.

Authors:  Maxwell S Stem; Bozho Todorich; Maria A Woodward; Jason Hsu; Jeremy D Wolfe
Journal:  J Vitreoretin Dis       Date:  2017-03-02

7.  Trends and characteristics of congenital ectopia lentis in China.

Authors:  Guang-Ming Jin; Min Fan; Qian-Zhong Cao; Jun-Xiong Lin; Yi-Chi Zhang; Jian-Qiang Lin; Yi-Yao Wang; Charlotte-Aimee Young; Dan-Ying Zheng
Journal:  Int J Ophthalmol       Date:  2018-09-18       Impact factor: 1.779

Review 8.  Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.

Authors:  Andrew A M Morris; Viktor Kožich; Saikat Santra; Generoso Andria; Tawfeg I M Ben-Omran; Anupam B Chakrapani; Ellen Crushell; Mick J Henderson; Michel Hochuli; Martina Huemer; Miriam C H Janssen; Francois Maillot; Philip D Mayne; Jenny McNulty; Tara M Morrison; Helene Ogier; Siobhan O'Sullivan; Markéta Pavlíková; Isabel Tavares de Almeida; Allyson Terry; Sufin Yap; Henk J Blom; Kimberly A Chapman
Journal:  J Inherit Metab Dis       Date:  2016-10-24       Impact factor: 4.982

9.  Mutation survey of candidate genes in 40 Chinese patients with congenital ectopia lentis.

Authors:  Jie Li; Xiaoyun Jia; Shiqiang Li; Shaohua Fang; Xiangming Guo
Journal:  Mol Vis       Date:  2014-07-18       Impact factor: 2.367

10.  Long-Term Suture Breakage After Scleral Fixation of a Modified Capsular Tension Ring with Polypropylene 10-0 Suture.

Authors:  Olav Kristianslund; Gunhild F Sandvik; Liv Drolsum
Journal:  Clin Ophthalmol       Date:  2021-06-14
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