Literature DB >> 15734019

Histopathologic study of X-linked cone-rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15.

F Yesim K Demirci1, Nisha Gupta, Amy L Radak, Brian W Rigatti, Tammy S Mah, Ann H Milam, Michael B Gorin.   

Abstract

PURPOSE: To evaluate the donor retina of a patient with X-linked cone-rod dystrophy caused by an RPGR exon ORF15 mutation.
DESIGN: Histopathologic study of the retina.
METHODS: The eye of a 69-year-old man was fixed at 1.6 hours postmortem and processed for histopathology and immunocytochemistry.
RESULTS: Grossly, the macula was atrophic with a bull's-eye appearance. The remaining retina showed postmortem edema but no intraretinal pigment. Microscopically, the macular retinal pigment epithelium was absent focally and had pigmentary changes elsewhere. Cones and rods were absent from the perifovea and reduced with shortened outer segments elsewhere in the macula. In the remainder of the retina, cones but not rods were reduced and all photoreceptor outer segments were shortened.
CONCLUSIONS: The abnormalities in both cone and rod photoreceptors confirm the importance of RPGR in both cell types but leaves unresolved how various exon ORF15 mutations lead to different clinical phenotypes.

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Year:  2005        PMID: 15734019     DOI: 10.1016/j.ajo.2004.08.041

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  10 in total

1.  Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa.

Authors:  William A Beltran; Artur V Cideciyan; Alfred S Lewin; Simone Iwabe; Hemant Khanna; Alexander Sumaroka; Vince A Chiodo; Diego S Fajardo; Alejandro J Román; Wen-Tao Deng; Malgorzata Swider; Tomas S Alemán; Sanford L Boye; Sem Genini; Anand Swaroop; William W Hauswirth; Samuel G Jacobson; Gustavo D Aguirre
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-23       Impact factor: 11.205

2.  RPGR-associated retinal degeneration in human X-linked RP and a murine model.

Authors:  Wei Chieh Huang; Alan F Wright; Alejandro J Roman; Artur V Cideciyan; Forbes D Manson; Dina Y Gewaily; Sharon B Schwartz; Sam Sadigh; Maria P Limberis; Peter Bell; James M Wilson; Anand Swaroop; Samuel G Jacobson
Journal:  Invest Ophthalmol Vis Sci       Date:  2012-08-15       Impact factor: 4.799

3.  Retrospective Natural History Study of RPGR-Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the Disease.

Authors:  Marco Nassisi; Giuseppe De Bartolo; Saddek Mohand-Said; Christel Condroyer; Aline Antonio; Marie-Elise Lancelot; Kinga Bujakowska; Vasily Smirnov; Thomas Pugliese; John Neidhardt; José-Alain Sahel; Christina Zeitz; Isabelle Audo
Journal:  Int J Mol Sci       Date:  2022-06-28       Impact factor: 6.208

4.  Targeting gene expression to cones with human cone opsin promoters in recombinant AAV.

Authors:  A M Komáromy; J J Alexander; A E Cooper; V A Chiodo; L G Glushakova; G M Acland; W W Hauswirth; G D Aguirre
Journal:  Gene Ther       Date:  2008-03-13       Impact factor: 5.250

5.  Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degeneration.

Authors:  Jason Charng; Artur V Cideciyan; Samuel G Jacobson; Alexander Sumaroka; Sharon B Schwartz; Malgorzata Swider; Alejandro J Roman; Rebecca Sheplock; Manisha Anand; Marc C Peden; Hemant Khanna; Elise Heon; Alan F Wright; Anand Swaroop
Journal:  Hum Mol Genet       Date:  2016-12-15       Impact factor: 6.150

6.  Cone-rod dystrophy can be a manifestation of Danon disease.

Authors:  Alberta A H J Thiadens; Niki W R Slingerland; Ralph J Florijn; Gerhard H Visser; Frans C Riemslag; Caroline C W Klaver
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2012-05       Impact factor: 3.117

7.  Detection of photoreceptor disruption by adaptive optics fundus imaging and Fourier-domain optical coherence tomography in eyes with occult macular dystrophy.

Authors:  Yoshiyuki Kitaguchi; Shunji Kusaka; Tatsuo Yamaguchi; Toshifumi Mihashi; Takashi Fujikado
Journal:  Clin Ophthalmol       Date:  2011-03-10

8.  Clinical course of cone dystrophy caused by mutations in the RPGR gene.

Authors:  Alberta A H J Thiadens; Gyan G Soerjoesing; Ralph J Florijn; A G Tjiam; Anneke I den Hollander; L Ingeborgh van den Born; Frans C Riemslag; Arthur A B Bergen; Caroline C W Klaver
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2011-08-25       Impact factor: 3.117

9.  Genotype-Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review.

Authors:  Junxing Yang; Lin Zhou; Jiamin Ouyang; Xueshan Xiao; Wenmin Sun; Shiqiang Li; Qingjiong Zhang
Journal:  Front Genet       Date:  2021-06-23       Impact factor: 4.599

10.  Cone Dystrophy Associated with a Novel Variant in the Terminal Codon of the RPGR-ORF15.

Authors:  Vlasta Hadalin; Maja Šuštar; Marija Volk; Aleš Maver; Jana Sajovic; Martina Jarc-Vidmar; Borut Peterlin; Marko Hawlina; Ana Fakin
Journal:  Genes (Basel)       Date:  2021-03-29       Impact factor: 4.096

  10 in total

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