Literature DB >> 32076389

Endothelial dysfunction in a child with Pearson marrow-pancreas syndrome managed with Descemet stripping automated endothelial keratoplasty using a suture pull-through technique.

Raghav Vadhul1, Caroline S Halbach2, Raymond G Areaux2, Susan Berry3, Joshua H Hou2.   

Abstract

A 4-year-old girl with a history of Pearson marrow-pancreas syndrome presenting with severe, progressive photophobia was found to have bilateral, diffuse corneal thickening and peripheral pigmentary retinopathy. She underwent Descemet stripping automated endothelial keratoplasty (DSAEK) surgery in both eyes using a modified suture pull-through technique. Postoperatively there was no evidence of cataract formation or graft detachment; her corneas thinned, and her photophobia improved dramatically.
Copyright ©2019. All rights reserved. Reproduction in whole or in part in any form or medium without expressed written permission of the Digital Journal of Ophthalmology is prohibited.

Entities:  

Year:  2019        PMID: 32076389      PMCID: PMC7001650          DOI: 10.5693/djo.02.2019.09.001

Source DB:  PubMed          Journal:  Digit J Ophthalmol        ISSN: 1542-8958


  2 in total

Review 1.  Pediatric endothelial keratoplasty: a systematic review and individual participant data meta-analysis.

Authors:  Masomeh Mohebbi; Mohammad Mehrpour; Amin Dehghani Sanij; Nader Mohammadi; Masoud Mirghorbani
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2021-10-28       Impact factor: 3.117

2.  Identification of a novel large deletion of the mitochondrial DNA in an infant with Pearson syndrome: a case report.

Authors:  Rui Liu; Gui-Ling Mo; Yuan-Zong Song
Journal:  Transl Pediatr       Date:  2021-01
  2 in total

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