Literature DB >> 900227

Central areolar choroidal dystrophy.

K G Noble.   

Abstract

Three members of a family with central areolar choroidal dystrophy showed the early and late stages of this disorder. The youngest affected was a 12-year-old girl who exhibited decreased vision, a red-green dyschromatopsia, and mild granularity of the macula with a diffuse foveal reflex. A discrete focal loss of choriocapillaris in the macula was seen on fluorescein angiography. This indicates that choriocapillaris atrophy is an early finding in this disease.

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Mesh：

Year:  1977        PMID： 900227     DOI： 10.1016/0002-9394(77)90670-5

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


  6 in total

1.  Electroretinograms and pattern visually evoked cortical potentials in central areolar choroidal dystrophy.

Authors:  E Adachi-Usami; K Murayama; Y Yamamoto
Journal:  Doc Ophthalmol       Date:  1990-08       Impact factor: 2.379

2.  The development of central areolar choroidal dystrophy.

Authors:  C B Hoyng; A F Deutman
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1996-02       Impact factor: 3.117

Review 3.  Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.

Authors:  A Iannaccone
Journal:  Doc Ophthalmol       Date:  2001-05       Impact factor: 2.379

4.  Polymorphous presentations in vitelliform macular dystrophy: subretinal neovascularisation and central choroidal atrophy.

Authors:  K G Noble; B M Scher; R E Carr
Journal:  Br J Ophthalmol       Date:  1978-08       Impact factor: 4.638

5.  New Insights on the Regulatory Gene Network Disturbed in Central Areolar Choroidal Dystrophy-Beyond Classical Gene Candidates.

Authors:  João Paulo Kazmierczak de Camargo; Giovanna Nazaré de Barros Prezia; Naoye Shiokawa; Mario Teruo Sato; Roberto Rosati; Angelica Beate Winter Boldt
Journal:  Front Genet       Date:  2022-05-17       Impact factor: 4.772

6.  Phenotypic Differences in a PRPH2 Mutation in Members of the Same Family Assessed with OCT and OCTA.

Authors:  Henar Albertos-Arranz; Xavier Sánchez-Sáez; Natalia Martínez-Gil; Isabel Pinilla; Rosa M Coco-Martin; Jesús Delgado; Nicolás Cuenca
Journal:  Diagnostics (Basel)       Date:  2021-04-26
  6 in total

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