Literature DB >> 17134646

Current concepts of ocular manifestations in Marfan syndrome.

Arie Y Nemet1, Ehud I Assia, David J Apple, Irina S Barequet.   

Abstract

Marfan syndrome is a widespread disorder of connective tissue. It is characterized by systemic and ocular features due to mutations in the fibrillin gene. Awareness and prompt recognition of the ocular complications of Marfan syndrome may enable improvement and preservation of sight. Studies have been performed in the last few years that enable a better understanding of the genetics of the syndrome, earlier diagnosis, and improvement in the surgical techniques and options.

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Year:  2006        PMID: 17134646     DOI: 10.1016/j.survophthal.2006.08.008

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


  29 in total

Review 1.  Keratoglobus.

Authors:  B S Wallang; S Das
Journal:  Eye (Lond)       Date:  2013-06-28       Impact factor: 3.775

Review 2.  Marfan syndrome. Part 1: pathophysiology and diagnosis.

Authors:  Victoria Cañadas; Isidre Vilacosta; Isidoro Bruna; Valentin Fuster
Journal:  Nat Rev Cardiol       Date:  2010-03-30       Impact factor: 32.419

Review 3.  Molecular pathogenesis and management strategies of ectopia lentis.

Authors:  A Chandra; D Charteris
Journal:  Eye (Lond)       Date:  2014-01-10       Impact factor: 3.775

4.  Recurrent spontaneous scleral rupture in Marfan's syndrome.

Authors:  Kiranmaye Turaga; Sirisha Senthil; Subhadra Jalali
Journal:  BMJ Case Rep       Date:  2016-05-19

5.  Visual outcomes after lensectomy and iris claw artisan intraocular lens implantation in patients with Marfan syndrome.

Authors:  Hossein Mohammad Rabie; Parviz Malekifar; Mohammad Ali Javadi; Danial Roshandel; Hamed Esfandiari
Journal:  Int Ophthalmol       Date:  2016-10-05       Impact factor: 2.031

Review 6.  Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes.

Authors:  Aman George; Tiziana Cogliati; Brian P Brooks
Journal:  Exp Eye Res       Date:  2020-02-04       Impact factor: 3.467

7.  A novel fibrillin 1 gene mutation leading to marfan syndrome with minimal cardiac features.

Authors:  E Martínez-Quintana; F Rodríguez-González; P Garay-Sánchez; A Tugores
Journal:  Mol Syndromol       Date:  2014-02-27

8.  Simultaneous extrusion and intrusion of a scleral buckle in a patient with Marfan's syndrome.

Authors:  K T Oyewole; A J Shortt; Y Ramkissoon; P M Sullivan
Journal:  BMJ Case Rep       Date:  2011-02-17

9.  Intracranial Migration of Silicone Delaying Life Saving Surgical Management: A Mimicker of Hemorrhage.

Authors:  Dani Sarohia; Ramin Javan; Salim Aziz
Journal:  J Radiol Case Rep       Date:  2016-08-31

10.  Correlation of the recurrent FBN1 mutation (c.364C>T) with a unique phenotype in a Chinese patient with Marfan syndrome.

Authors:  Chongfei Jin; Ke Yao; Zhaohui Sun; Renyi Wu
Journal:  Jpn J Ophthalmol       Date:  2008-12-17       Impact factor: 2.447

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