Results 81 to 90 of about 3,283 (186)

Pars Plana Lensectomy Combined with Pars Plana Vitrectomy in Traumatic Ectopia Lentis

open access: yesBeyoglu Eye Journal, 2017
INTRODUCTION[|]The aim of the present study was to report the outcomes of pars plana lensectomy (PPL) combined with pars plana vitrectomy (PPV) in traumatic ectopia lentis performed at a tertiary eye hospital.[¤]METHODS[|]Patients who underwent PPL ...
Dilek Yasa
doaj   +1 more source

ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians

open access: yes, 2017
BACKGROUND:To clinically characterize a cohort of patients with ectopia lentis (EL), or Marfanoid features in whom a definite genetic diagnosis of Marfan syndrome (MFS) had been excluded (atypical MFS), and to evaluate the contribution of mutations in ...
Ikink, Will   +9 more
core   +1 more source

Marfan syndrome associated to pectus carinatum: a case report from cartagena de indias. Colombia

open access: yesRevista Ciencias Biomédicas, 2011
Marfan syndrome (MFS) is the most common connective tissue inherited disorder,transmitted as an autosomic dominant character. Mutation is located in FBN1 allele,that encodes to Fibrilin-1.
Malambo-García Dacia I   +4 more
doaj  

Poster Sessions

open access: yes
HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Bilateral simple ectopia lentis

open access: yesIndian Journal of Ophthalmology. Case Reports, 2023
Shagun Korla, Ravinder K Gupta
doaj   +1 more source

A CASE OF CONGENITAL ECTOPIA LENTIS [PDF]

open access: yesThe American Journal of the Medical Sciences, 1885
n ...
openaire   +1 more source

A Pedigree Report of a Rare Case of Weill–Marchesani Syndrome with New Compound Heterozygous LTBP2 Mutations

open access: yesRisk Management and Healthcare Policy, 2021
ZhiHong Lin,* MinJuan Zhu,* HongWei Deng Department of Strabismus & Pediatric Ophthalmology, Shenzhen Eye Hospital Affiliated to Jinan University, The School of Optometry of Shenzhen University, Shenzhen, 518000, Guangdong Province, People’s ...
Lin Z, Zhu M, Deng H
doaj  

Autosomal recessive bilateral frontal polymicrogyria with ectopia lentis and chorioretinal dystrophy

open access: yes, 2013
Polymicrogyria is a type of cortical dysplasia with cortical organizational defect. Bilateral polymicrogyria are distinct with genetic basis in a subset.
Sribhargava Natesh   +4 more
core   +1 more source

sj-docx-3-ejo-10.1177_11206721241242158 - Supplemental material for Scleral-fixated vs Iris-fixated intraocular lens in pediatric ectopia lentis: A systematic review

open access: yes
Supplemental material, sj-docx-3-ejo-10.1177_11206721241242158 for Scleral-fixated vs Iris-fixated intraocular lens in pediatric ectopia lentis: A systematic review by Siti Halida Zoraida Soraya Alamsjah, Dian Estu Yulia and Sabrina Tan in European ...
Siti Halida Zoraida Soraya Alamsjah (18266490)   +2 more
core   +1 more source

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