Literature DB >> 9683165

Histopathologic and immunohistochemical study of dominant cone degeneration.

K To1, M Adamian, F A Jakobiec, E L Berson.   

Abstract

PURPOSE: To report the histopathologic and immunohistochemical findings in autosomal dominant cone degeneration.
METHODS: The autopsy eyes of a 75-year-old man with autosomal dominant cone degeneration were studied with both light and electron microscopy. In addition, immunofluorescent studies using antibodies to cone opsins and cone alpha transducin were performed.
RESULTS: Histopathologic examination of the fovea disclosed loss of photoreceptors and attenuated retinal pigment epithelium. Reduced numbers of cones could be seen in the parafovea, and only occasional cones were visible in the periphery; rods were preserved in the periphery.
CONCLUSION: The histopathologic and immunohistochemical findings in this case of dominantly inherited cone degeneration correlate well with the loss of cone function and preservation of normal or nearly normal rod function upon clinical examination. This condition affects red, green, and blue cones.

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Year:  1998        PMID: 9683165     DOI: 10.1016/s0002-9394(98)00085-3

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


  4 in total

1.  A G86R mutation in the calcium-sensor protein GCAP1 alters regulation of retinal guanylyl cyclase and causes dominant cone-rod degeneration.

Authors:  Igor V Peshenko; Artur V Cideciyan; Alexander Sumaroka; Elena V Olshevskaya; Alexander Scholten; Seher Abbas; Karl-Wilhelm Koch; Samuel G Jacobson; Alexander M Dizhoor
Journal:  J Biol Chem       Date:  2019-01-08       Impact factor: 5.157

2.  A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degeneration.

Authors:  Koji M Nishiguchi; Izabela Sokal; Lili Yang; Nirmalya Roychowdhury; Krzysztof Palczewski; Eliot L Berson; Thaddeus P Dryja; Wolfgang Baehr
Journal:  Invest Ophthalmol Vis Sci       Date:  2004-11       Impact factor: 4.799

3.  Use of spectral domain-optical coherence tomography to visualize photoreceptor abnormalities in cone-rod dystrophy 6.

Authors:  Ben J Kim; Mohamed A Ibrahim; Morton F Goldberg
Journal:  Retin Cases Brief Rep       Date:  2011

4.  Phenotypic diversity in autosomal-dominant cone-rod dystrophy elucidated by adaptive optics retinal imaging.

Authors:  Hongxin Song; Ethan A Rossi; Edwin Stone; Lisa Latchney; David Williams; Alfredo Dubra; Mina Chung
Journal:  Br J Ophthalmol       Date:  2017-10-26       Impact factor: 4.638

  4 in total

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