Literature DB >> 21376398

Congenital aniridia variant: minimally abnormal irides with severe limbal stem cell deficiency.

Heather M Skeens1, Brian P Brooks, Edward J Holland.   

Abstract

PURPOSE: To clinically and molecularly characterize a group of patients with progressive limbal stem cell deficiency (LSCD) due to aniridic keratopathy (AK), but with minimally affected irides.
DESIGN: Retrospective case series. PARTICIPANTS: A total of 12 eyes of 6 patients who underwent keratolimbal allograft (KLAL) for AK in the absence of the classic stigmata of aniridia at the Cincinnati Eye Institute/University of Cincinnati between 2000 and 2007.
METHODS: Retrospective chart review. MAIN OUTCOME MEASURES: Ocular surface stability after KLAL and change in visual acuity.
RESULTS: Subjects' mean age was 32.57 years, 66% were female, and mean follow-up was 64.4 months (range, 20-115 months). All patients presented with a decline in their vision secondary to LSCD. Average preoperative best-corrected visual acuity (BCVA) logarithm of the minimum angle of resolution (logMAR) was 1.4 (range, 0.10-2.8). All patients had minimally affected irides with subtle abnormal findings, including ectropion uveae and stromal atrophy. All patients developed severe LSCD and required KLAL. Average postoperative logMAR BCVA was 0.35 (range, 0.00-1.00). All ocular surfaces remained stable throughout the follow-up period. Family history consistent with autosomal dominant inheritance was positive in 4 of 6 patients. PAX6 genetic testing identified 2 pathologic mutations and 1 possible disease-causing variant.
CONCLUSIONS: Aniridic keratopathy may present in the absence of other classic stigmata of aniridia and be associated with minimally affected irides. A subset of these patients has definitive mutations in PAX6 and once identified can be counseled appropriately. These patients respond well to KLAL and may therefore benefit from early detection.
Copyright © 2011 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21376398     DOI: 10.1016/j.ophtha.2010.11.021

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  15 in total

1.  Implication of non-coding PAX6 mutations in aniridia.

Authors:  Julie Plaisancié; M Tarilonte; P Ramos; C Jeanton-Scaramouche; V Gaston; H Dollfus; D Aguilera; J Kaplan; L Fares-Taie; F Blanco-Kelly; C Villaverde; C Francannet; A Goldenberg; I Arroyo; J M Rozet; C Ayuso; N Chassaing; P Calvas; M Corton
Journal:  Hum Genet       Date:  2018-10-05       Impact factor: 4.132

2.  Functional reassessment of PAX6 single nucleotide variants by in vitro splicing assay.

Authors:  Alexandra Yu Filatova; Tatiana A Vasilyeva; Andrey V Marakhonov; Anna A Voskresenskaya; Rena A Zinchenko; Mikhail Yu Skoblov
Journal:  Eur J Hum Genet       Date:  2018-10-12       Impact factor: 4.246

3.  In vivo confocal microscopy of congenital aniridia-associated keratopathy.

Authors:  Q Le; S X Deng; J Xu
Journal:  Eye (Lond)       Date:  2013-04-12       Impact factor: 3.775

4.  Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.

Authors:  Lubica Dudakova; Sek-Shir Cheong; Stanislava Reinstein Merjava; Pavlina Skalicka; Marcela Michalickova; Michalis Palos; Gabriela Mahelkova; Deli Krizova; Martin Hlozanek; Marie Trkova; Jena L Chojnowski; Enkela Hrdlickova; Nikolas Pontikos; Vincent Plagnol; Viera Veselá; Katerina Jirsova; Alison J Hardcastle; Martin Filipec; James D Lauderdale; Petra Liskova
Journal:  Stem Cell Rev Rep       Date:  2018-02       Impact factor: 5.739

5.  Global Consensus on Definition, Classification, Diagnosis, and Staging of Limbal Stem Cell Deficiency.

Authors:  Sophie X Deng; Vincent Borderie; Clara C Chan; Reza Dana; Francisco C Figueiredo; José A P Gomes; Graziella Pellegrini; Shigeto Shimmura; Friedrich E Kruse
Journal:  Cornea       Date:  2019-03       Impact factor: 2.651

6.  [Stage-related therapy of congenital aniridia].

Authors:  B Seitz; B Käsmann-Kellner; A Viestenz
Journal:  Ophthalmologe       Date:  2014-12       Impact factor: 1.059

Review 7.  The diagnosis of limbal stem cell deficiency.

Authors:  Qihua Le; Jianjiang Xu; Sophie X Deng
Journal:  Ocul Surf       Date:  2017-11-04       Impact factor: 5.033

8.  Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease.

Authors:  Claudia Yahalom; Anat Blumenfeld; Karen Hendler; Orly Wussuki-Lior; Michal Macarov; Mordechai Shohat; Samer Khateb
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2018-08-30       Impact factor: 3.117

9.  Congenital aniridia: etiology, manifestations and management.

Authors:  Monica Samant; Bharesh K Chauhan; Kira L Lathrop; Ken K Nischal
Journal:  Expert Rev Ophthalmol       Date:  2016-03-09

Review 10.  Presentation, diagnosis and management of limbal stem cell deficiency.

Authors:  Kunjal Sejpal; Pejman Bakhtiari; Sophie X Deng
Journal:  Middle East Afr J Ophthalmol       Date:  2013 Jan-Mar
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