Cargando…
Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy
Bietti’s crystalline dystrophy (BCD) consists of small, yellow-white, glistening intraretinal crystals in the posterior pole, tapetoretinal degeneration with atrophy of the retinal pigment epithelium (RPE) and “sclerosis” of the choroid; in addition, sparking yellow crystals in the superficial margi...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045089/ https://www.ncbi.nlm.nih.gov/pubmed/21359135 |
_version_ | 1782198795185946624 |
---|---|
author | Furusato, Emiko Cameron, J. Douglas Chan, Chi-Chao |
author_facet | Furusato, Emiko Cameron, J. Douglas Chan, Chi-Chao |
author_sort | Furusato, Emiko |
collection | PubMed |
description | Bietti’s crystalline dystrophy (BCD) consists of small, yellow-white, glistening intraretinal crystals in the posterior pole, tapetoretinal degeneration with atrophy of the retinal pigment epithelium (RPE) and “sclerosis” of the choroid; in addition, sparking yellow crystals in the superficial marginal cornea are also found in many patients. BCD is inherited as an autosomal-recessive trait (4q35-tel) and usually has its onset in the third decade of life. This review focuses on the ultrastructure of cellular crystals and lipid inclusions of BCD. |
format | Text |
id | pubmed-3045089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-30450892011-02-25 Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy Furusato, Emiko Cameron, J. Douglas Chan, Chi-Chao Ophthalmol Eye Dis Review Bietti’s crystalline dystrophy (BCD) consists of small, yellow-white, glistening intraretinal crystals in the posterior pole, tapetoretinal degeneration with atrophy of the retinal pigment epithelium (RPE) and “sclerosis” of the choroid; in addition, sparking yellow crystals in the superficial marginal cornea are also found in many patients. BCD is inherited as an autosomal-recessive trait (4q35-tel) and usually has its onset in the third decade of life. This review focuses on the ultrastructure of cellular crystals and lipid inclusions of BCD. Libertas Academica 2010-03-09 /pmc/articles/PMC3045089/ /pubmed/21359135 Text en © 2010 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited. |
spellingShingle | Review Furusato, Emiko Cameron, J. Douglas Chan, Chi-Chao Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title | Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title_full | Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title_fullStr | Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title_full_unstemmed | Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title_short | Evolution of Cellular Inclusions in Bietti’s Crystalline Dystrophy |
title_sort | evolution of cellular inclusions in bietti’s crystalline dystrophy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3045089/ https://www.ncbi.nlm.nih.gov/pubmed/21359135 |
work_keys_str_mv | AT furusatoemiko evolutionofcellularinclusionsinbiettiscrystallinedystrophy AT cameronjdouglas evolutionofcellularinclusionsinbiettiscrystallinedystrophy AT chanchichao evolutionofcellularinclusionsinbiettiscrystallinedystrophy |