Literature DB >> 18090894

Pathophysiology of zonular diseases.

Pascal Dureau1.   

Abstract

PURPOSE OF REVIEW: The mechanisms implicated in the clinical manifestations of zonular diseases, especially ectopia lentis, are reviewed. RECENT
FINDINGS: The molecular mechanisms involve fibrillin in a large spectrum of heritable diseases characterized by zonular stretching. The usual complications are refractive errors, especially myopia, glaucoma (either primary open angle, secondary angle closure and pupil block by anterior displacement of the lens) and retinal detachment.
SUMMARY: The genetics and molecular understanding provide information for genetic counseling. Treatment of myopia and glaucoma depend on the underlying mechanism, and lens surgery techniques are continuously improved.

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Year:  2008        PMID: 18090894     DOI: 10.1097/ICU.0b013e3282f29f01

Source DB:  PubMed          Journal:  Curr Opin Ophthalmol        ISSN: 1040-8738            Impact factor:   3.761


  19 in total

1.  [Bilateral ciliary zonule defect].

Authors:  H Neunhöffer; L Goldammer; V Gravenhorst; N Feltgen; H Hoerauf
Journal:  Ophthalmologe       Date:  2011-07       Impact factor: 1.059

Review 2.  [Secondary diseases in high myopia].

Authors:  F Ziemssen; W Lagrèze; B Voykov
Journal:  Ophthalmologe       Date:  2017-01       Impact factor: 1.059

3.  Latent TGF-β binding protein-2 is essential for the development of ciliary zonule microfibrils.

Authors:  Tadashi Inoue; Tetsuya Ohbayashi; Yusuke Fujikawa; Hideyuki Yoshida; Tomoya O Akama; Kazuo Noda; Masahito Horiguchi; Katsuro Kameyama; Yoshio Hata; Kanji Takahashi; Kenji Kusumoto; Tomoyuki Nakamura
Journal:  Hum Mol Genet       Date:  2014-06-06       Impact factor: 6.150

Review 4.  Genetics of thoracic aortic aneurysms.

Authors:  Guillaume Jondeau; Catherine Boileau
Journal:  Curr Atheroscler Rep       Date:  2012-06       Impact factor: 5.113

5.  LTBP2 and CYP1B1 mutations and associated ocular phenotypes in the Roma/Gypsy founder population.

Authors:  Dimitar N Azmanov; Stanislava Dimitrova; Laura Florez; Sylvia Cherninkova; Dragomir Draganov; Bharti Morar; Rosmawati Saat; Manel Juan; Juan I Arostegui; Sriparna Ganguly; Himla Soodyall; Subhabrata Chakrabarti; Harish Padh; Miguel A López-Nevot; Violeta Chernodrinska; Botio Anguelov; Partha Majumder; Lyudmila Angelova; Radka Kaneva; David A Mackey; Ivailo Tournev; Luba Kalaydjieva
Journal:  Eur J Hum Genet       Date:  2010-11-17       Impact factor: 4.246

6.  Biological Preparation and Mechanical Technique for Determining Viscoelastic Properties of Zonular Fibers.

Authors:  Juan Rodriguez; Matthew Reilly; Robert P Mecham; Steven Bassnett
Journal:  J Vis Exp       Date:  2021-12-16       Impact factor: 1.424

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

8.  Mapping of the disease locus and identification of ADAMTS10 as a candidate gene in a canine model of primary open angle glaucoma.

Authors:  John Kuchtey; Lana M Olson; Tommy Rinkoski; Edward O Mackay; T M Iverson; Kirk N Gelatt; Jonathan L Haines; Rachel W Kuchtey
Journal:  PLoS Genet       Date:  2011-02-17       Impact factor: 5.917

9.  Prevalence of zonulopathy in primary angle closure disease.

Authors:  Ali Salimi; Anthony Fanous; Harrison Watt; Mohamed Abu-Nada; Anna Wang; Paul Harasymowycz
Journal:  Clin Exp Ophthalmol       Date:  2021-08-31       Impact factor: 4.383

10.  C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family.

Authors:  Fengyun Wang; Bo Li; Lan Lan; Lin Li
Journal:  Mol Vis       Date:  2015-02-23       Impact factor: 2.367

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