Literature DB >> 19724202

In vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase deficiency.

Pat-Michael Palmiero1, Zaher Sbeity, Jeffrey Liebmann, Robert Ritch.   

Abstract

PURPOSE: To report high-resolution, in vivo imaging of the cornea in a patient with lecithin-cholesterol acyltransferase (LCAT) deficiency.
METHODS: A 60-year-old Ecuadorian woman with bilateral corneal opacities and confirmed LCAT deficiency was imaged with Fourier domain optical coherence tomography (FD-OCT) and noncontact Rostock confocal laser scanning microscopy.
RESULTS: The FD-OCT revealed a thinned epithelium, homogeneous hyperreflective stroma, and focal disruptions of Bowman's layer. Focal areas of hyperreflectivity with multiple dark striae and reduced and irregular keratocytes were seen throughout the stroma by noncontact Rostock module. The corneal endothelium was normal.
CONCLUSION: New anterior segment in vivo imaging technology permits high-resolutional visualization and monitoring of corneal pathology.

Entities:  

Mesh:

Year:  2009        PMID: 19724202     DOI: 10.1097/ICO.0b013e31819839ae

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  7 in total

1.  A woman with low HDL cholesterol and corneal opacity.

Authors:  Tiziano Lucchi; Laura Calabresi; Angela Pinto; Elisa Benetti; Beatrice Arosio; Sara Simonelli; Roberto Ratiglia; Carlo Vergani
Journal:  Intern Emerg Med       Date:  2011-10-29       Impact factor: 3.397

2.  Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement.

Authors:  Robert D Shamburek; Rebecca Bakker-Arkema; Bruce J Auerbach; Brian R Krause; Reynold Homan; Marcelo J Amar; Lita A Freeman; Alan T Remaley
Journal:  J Clin Lipidol       Date:  2015-12-23       Impact factor: 4.766

Review 3.  Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature.

Authors:  Bijan Roshan; Om P Ganda; Ranil Desilva; Rose B Ganim; Edmund Ward; Sarah D Haessler; Eliana Y Polisecki; Bela F Asztalos; Ernst J Schaefer
Journal:  J Clin Lipidol       Date:  2011-08-23       Impact factor: 4.766

4.  Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers.

Authors:  I Castro-Ferreira; Rute Carmo; Sérgio Estrela Silva; Otília Corrêa; Susana Fernandes; Susana Sampaio; Rodrigues-Pereira Pedro; Augusta Praça; João Paulo Oliveira
Journal:  JIMD Rep       Date:  2017-10-06

5.  Clinical features and visual function in a patient with Fish-eye disease: Quantitative measurements and optical coherence tomography.

Authors:  Masanori Kanai; Shizuka Koh; Daisaku Masuda; Masahiro Koseki; Kohji Nishida
Journal:  Am J Ophthalmol Case Rep       Date:  2018-02-24

6.  Corneal thickness in the case of familial lecithin-cholesterol acyltransferase deficiency.

Authors:  Shinsuke Kinoshita; Seiichiro Sugita; Akihiro Yoshida
Journal:  Am J Ophthalmol Case Rep       Date:  2021-09-21

7.  LCAT deficiency: a systematic review with the clinical and genetic description of Mexican kindred.

Authors:  Roopa Mehta; Daniel Elías-López; Alexandro J Martagón; Oscar A Pérez-Méndez; Maria Luisa Ordóñez Sánchez; Yayoi Segura; Maria Teresa Tusié; Carlos A Aguilar-Salinas
Journal:  Lipids Health Dis       Date:  2021-07-13       Impact factor: 3.876

  7 in total

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