Literature DB >> 3489456

X-linked recessive cone dystrophy with tapetal-like sheen. A newly recognized entity with Mizuo-Nakamura phenomenon.

J R Heckenlively, R G Weleber.   

Abstract

We encountered a new X-linked recessive cone dystrophy in which patients have a greenish-golden tapetal-like sheen of the retina; while the retinal sheen and electroretinographic abnormalities are present from childhood, patients are not symptomatic until adult years. All of the male patients tested showed evidence of cone dysfunction on color vision testing, dark adaptometry, and electroretinography. After three hours of dark adaptation, the tapetal-like sheen disappeared, with most areas changing from greenish-golden shades to orange-red hues (Mizuo-Nakamura phenomenon). One male patient had a retinal detachment from atrophic round holes in the equatorial retina.

Entities:  

Mesh:

Year:  1986        PMID: 3489456     DOI: 10.1001/archopht.1986.01050210076029

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  15 in total

1.  Evolution of the tapetum.

Authors:  Ivan R Schwab; Carlton K Yuen; Nedim C Buyukmihci; Thomas N Blankenship; Paul G Fitzgerald
Journal:  Trans Am Ophthalmol Soc       Date:  2002

2.  Cone and cone-rod dystrophies.

Authors:  A T Moore
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  X linked progressive cone dystrophy with specific attention to carrier detection.

Authors:  J A van Everdingen; L N Went; J E Keunen; J A Oosterhuis
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

4.  X-linked cone dystrophy.

Authors:  C Verdoorn; A Pinckers
Journal:  Doc Ophthalmol       Date:  1988 Oct-Nov       Impact factor: 2.379

5.  A 34-year-old man with visual complaints and a tapetal-like reflex.

Authors:  Joao C M L Ribeiro; Cynthia S Chiu; Christine Ament; John I Loewenstein
Journal:  Digit J Ophthalmol       Date:  2008-07-28

6.  X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.

Authors:  R Jalkanen; M Mäntyjärvi; R Tobias; J Isosomppi; E-M Sankila; T Alitalo; N T Bech-Hansen
Journal:  J Med Genet       Date:  2006-02-27       Impact factor: 6.318

7.  Psychosocial genetics: an emerging scientific discipline.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

8.  A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.

Authors:  Maleeha Azam; Rob W J Collin; Muhammad Imran Khan; Syed Tahir Abbas Shah; Nadeem Qureshi; Muhammad Ajmal; Anneke I den Hollander; Raheel Qamar; Frans P M Cremers
Journal:  Mol Vis       Date:  2009-09-05       Impact factor: 2.367

9.  Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).

Authors:  H K Hong; R E Ferrell; M B Gorin
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

10.  X linked progressive cone dystrophy. Localisation of the gene locus to Xp21-p11.1 by linkage analysis.

Authors:  F M Meire; A A Bergen; A De Rouck; M Leys; J W Delleman
Journal:  Br J Ophthalmol       Date:  1994-02       Impact factor: 4.638

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