Literature DB >> 306693

Bietti's tapetoretinal degeneration with marginal corneal dystrophy crystalline retinopathy.

R B Welch.   

Abstract

In 1937 Bietti reported a tapetoretinal degeneration with associated corneal deposits at the limbus. The hallmark of the disease was the crystalline characteristics of the retinal spots as well as those at the corneal limbus. Bagolini and Ioli-Spade in 1968 presented a 30 year follow-up on Bietti's cases and presented six additional cases. The present report delas with this entity in Orientals, a Chinese woman and a Japanese man. Corneal and conjunctival biopsy from the female patient revelaed a lipid deposition in both fibroblasts and epithelium. The term "crystalline retinopathy" has been added to the description of this entity since it defines the most characteristic feature of the syndrome.

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Year:  1977        PMID: 306693      PMCID: PMC1311548     

Source DB:  PubMed          Journal:  Trans Am Ophthalmol Soc        ISSN: 0065-9533


  1 in total

1.  Tapetoretinal degeneration: report of four cases of a rare form of luminescent crystalline tapetoretinal degeneration; with a discussion of its cause.

Authors:  J LIJO PAVIA
Journal:  Am J Ophthalmol       Date:  1953-10       Impact factor: 5.258

  1 in total
  15 in total

Review 1.  The differential diagnosis of crystals in the retina.

Authors:  F Nadim; H Walid; J Adib
Journal:  Int Ophthalmol       Date:  2001       Impact factor: 2.031

2.  Functional and clinical findings in 3 female siblings with crystalline retinopathy.

Authors:  Hongling Chen; Mingzhi Zhang; Shizhou Huang; Dezheng Wu
Journal:  Doc Ophthalmol       Date:  2007-10-26       Impact factor: 2.379

3.  Bietti's crystalline dystrophy in Asians: clinical, angiographic and electrophysiological characteristics.

Authors:  Audra Mei Yee Fong; Adrian Koh; Kelvin Lee; Chong Lye Ang
Journal:  Int Ophthalmol       Date:  2008-10-15       Impact factor: 2.031

Review 4.  Ocular cytochrome P450s and transporters: roles in disease and endobiotic and xenobiotic disposition.

Authors:  Mariko Nakano; Catherine M Lockhart; Edward J Kelly; Allan E Rettie
Journal:  Drug Metab Rev       Date:  2014-05-26       Impact factor: 4.518

5.  Bietti crystalline retinal dystrophy with subfoveal neurosensory detachment and congenital tortuosity of retinal vessels: case report.

Authors:  Tapas Ranjan Padhi; Siddharth Kesarwani; Subhadra Jalali
Journal:  Doc Ophthalmol       Date:  2011-05-25       Impact factor: 2.379

6.  Evolution of Cellular Inclusions in Bietti's Crystalline Dystrophy.

Authors:  Emiko Furusato; J Douglas Cameron; Chi-Chao Chan
Journal:  Ophthalmol Eye Dis       Date:  2010-03-09

7.  A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti's crystalline dystrophy.

Authors:  Yanping Song; Guoyan Mo; Guohua Yin
Journal:  Int Ophthalmol       Date:  2012-12-14       Impact factor: 2.031

8.  Bietti's tapetoretinal degeneration with marginal corneal dystrophy (crystalline retinopathy): case report.

Authors:  R J Harrison; R R Acheson; J C Dean-Hart
Journal:  Br J Ophthalmol       Date:  1987-03       Impact factor: 4.638

9.  Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.

Authors:  Anren Li; Xiaodong Jiao; Francis L Munier; Daniel F Schorderet; Wenliang Yao; Fumino Iwata; Mutsuko Hayakawa; Atsushi Kanai; Muh Shy Chen; Richard Alan Lewis; John Heckenlively; Richard G Weleber; Elias I Traboulsi; Qingjiong Zhang; Xueshan Xiao; Muriel Kaiser-Kupfer; Yuri V Sergeev; J Fielding Hejtmancik
Journal:  Am J Hum Genet       Date:  2004-03-23       Impact factor: 11.025

10.  Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations.

Authors:  Yuuki Arai; Akiko Maeda; Yasuhiko Hirami; Chie Ishigami; Shinji Kosugi; Michiko Mandai; Yasuo Kurimoto; Masayo Takahashi
Journal:  J Ophthalmol       Date:  2015-06-16       Impact factor: 1.909

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