Literature DB >> 24406422

Molecular pathogenesis and management strategies of ectopia lentis.

A Chandra1, D Charteris2.   

Abstract

Ectopia lentis (EL) is a condition that can either herald underlying systemic conditions, or be isolated. The recent expansion in the genetics of these conditions has furthered the understanding of the underlying molecular aetiology. It is becoming apparent that novel genes, and in particular the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) family, are important in ocular development. The common link in these genes seems to be EL. The clinical management of EL is challenging. In particular, the options for addressing surgically induced aphakia in the context of an ectopic capsule are varied. Little evidence exists to direct management of these issues. This review summarises the molecular pathogenesis of EL and conditions associated with it, using the genetic aetiology as a framework. Furthermore, it summarises some of the issues involved in its clinical management.

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Year:  2014        PMID: 24406422      PMCID: PMC3930276          DOI: 10.1038/eye.2013.274

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN: 0950-222X            Impact factor:   3.775


  72 in total

Review 1.  Current concepts of ocular manifestations in Marfan syndrome.

Authors:  Arie Y Nemet; Ehud I Assia; David J Apple; Irina S Barequet
Journal:  Surv Ophthalmol       Date:  2006 Nov-Dec       Impact factor: 6.048

2.  Immunohistochemical evaluation of conjunctival fibrillin-1 in Marfan syndrome.

Authors:  Anuradha Ganesh; Charles Smith; Wilson Chan; Sheila Unger; Nada Quercia; Maurice Godfrey; Stephen Kraft; Raymond Buncic; Alex Levin
Journal:  Arch Ophthalmol       Date:  2006-02

3.  Lens subluxation and retinal dysfunction in a girl with homozygous VSX2 mutation.

Authors:  Arif O Khan; Mohammed A Aldahmesh; Jawaher Noor; Ahmed Salem; Fowzan S Alkuraya
Journal:  Ophthalmic Genet       Date:  2013-09-03       Impact factor: 1.803

4.  A novel ADAMTSL4 mutation in autosomal recessive ectopia lentis et pupillae.

Authors:  Anne E Christensen; Torunn Fiskerstrand; Per M Knappskog; Helge Boman; Eyvind Rødahl
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-08-11       Impact factor: 4.799

5.  Ectopia lentis et pupillae in four generations caused by novel mutations in the ADAMTSL4 gene.

Authors:  Yassi Sharifi; Martha J Tjon-Fo-Sang; Johannes R M Cruysberg; Anneke J Maat-Kievit
Journal:  Br J Ophthalmol       Date:  2013-02-20       Impact factor: 4.638

Review 6.  Ectopia lentis phenotypes and the FBN1 gene.

Authors:  Lesley C Adès; Katherine J Holman; Maggie S Brett; Matthew J Edwards; Bruce Bennetts
Journal:  Am J Med Genet A       Date:  2004-04-30       Impact factor: 2.802

7.  The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18.

Authors:  Mohammed A Aldahmesh; Muneera J Alshammari; Arif O Khan; Jawahir Y Mohamed; Fatimah A Alhabib; Fowzan S Alkuraya
Journal:  Hum Mutat       Date:  2013-07-19       Impact factor: 4.878

Review 8.  Clinical features of the congenital vitreoretinopathies.

Authors:  A O Edwards
Journal:  Eye (Lond)       Date:  2008-02-29       Impact factor: 3.775

9.  Identification of a major microfibril-associated glycoprotein-1-binding domain in fibrillin-2.

Authors:  Claudio C Werneck; Barbara Crippes Trask; Thomas J Broekelmann; Timothy M Trask; Timothy M Ritty; Fernando Segade; Robert P Mecham
Journal:  J Biol Chem       Date:  2004-03-24       Impact factor: 5.157

10.  The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.

Authors:  Ivana Peluso; Ivan Conte; Francesco Testa; Gopuraja Dharmalingam; Mariateresa Pizzo; Rob W J Collin; Nicola Meola; Sara Barbato; Margherita Mutarelli; Carmela Ziviello; Anna Maria Barbarulo; Vincenzo Nigro; Mariarosa A B Melone; Francesca Simonelli; Sandro Banfi
Journal:  Orphanet J Rare Dis       Date:  2013-01-28       Impact factor: 4.123

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  11 in total

1.  Are patients with ectopia lentis known to cardiology services?

Authors:  P Maghsoudlou; T Khanam; P J Banerjee; A Chandra
Journal:  Eye (Lond)       Date:  2018-11-05       Impact factor: 3.775

Review 2.  Non-cardiac manifestations of Marfan syndrome.

Authors:  Anne H Child
Journal:  Ann Cardiothorac Surg       Date:  2017-11

3.  Cell atlas of the human ocular anterior segment: Tissue-specific and shared cell types.

Authors:  Tavé van Zyl; Wenjun Yan; Alexi M McAdams; Aboozar Monavarfeshani; Gregory S Hageman; Joshua R Sanes
Journal:  Proc Natl Acad Sci U S A       Date:  2022-07-15       Impact factor: 12.779

4.  NGS analysis in Marfan syndrome spectrum: Combination of rare and common genetic variants to improve genotype-phenotype correlation analysis.

Authors:  Davide Gentilini; Antonino Oliveri; Teresa Fazia; Alessandro Pini; Susan Marelli; Luisa Bernardinelli; Anna Maria Di Blasio
Journal:  PLoS One       Date:  2019-09-19       Impact factor: 3.240

5.  Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis.

Authors:  Yijing Zhou; Dongwei Guo; Qianzhong Cao; Xinyu Zhang; Guangming Jin; Danying Zheng
Journal:  Mol Med Rep       Date:  2021-02-12       Impact factor: 2.952

6.  Recurrent Intraocular Lens Dislocation in a Patient with Familial Ectopia Lentis.

Authors:  Tomasz K Wilczyński; Alfred Niewiem; Rafał Leszczyński; Katarzyna Michalska-Małecka
Journal:  Int J Environ Res Public Health       Date:  2021-04-25       Impact factor: 3.390

7.  Retrospective study on the incidence of pseudoexfoliatio lentis and related complications in a cohort of patients from the Island of Ischia: medico-legal and ergophthalmology considerations.

Authors:  Mauro Salducci; Francesco Maiorano; Carmen Rachele Maione; Concetta Nappi; Marzio Di Meglio
Journal:  Rom J Ophthalmol       Date:  2021 Jul-Sep

8.  Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis.

Authors:  Jonas Gustafson; Maria Bjork; Conny M A van Ravenswaaij-Arts; Michael L Cunningham
Journal:  Case Rep Genet       Date:  2022-03-26

9.  Whole-exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family.

Authors:  Cheng Lei; Ting Guo; Shuizi Ding; Liyan Liao; Hong Peng; Zhiping Tan; Hong Luo
Journal:  Mol Genet Genomic Med       Date:  2020-11-20       Impact factor: 2.183

10.  How far is observation allowed in patients with ectopia lentis?

Authors:  Toshihiko Matsuo
Journal:  Springerplus       Date:  2015-08-28
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