Literature DB >> 7880798

Clinical pathology and retinal vascular structure in the Bardet-Biedl syndrome.

T Bek1, T Rosenberg.   

Abstract

A comparative study of clinical pathology and retinal vascular structure is described as studied by vascular casting in an eye of a patient with the Bardet-Biedl syndrome. At the time of examination the eye had been almost blind for at least 4 years. The histopathological examination showed a largely uniform loss of the outer retinal layers. The gross pathological examination of the cast ocular fundus showed three distinct zones, an inner zone inside the temporal vascular arcades where retinal vessels had been cast, a mid peripheral zone with bone spicules, and a peripheral zone with neither cast vessels nor bone spicules. The findings are discussed in relation to possible pathophysiological mechanisms involved in the development of retinal dystrophy in the Bardet-Biedl syndrome.

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Year:  1995        PMID: 7880798      PMCID: PMC505025          DOI: 10.1136/bjo.79.1.76

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  13 in total

1.  The Laurence-Moon-Biedl syndrome. Report of a typical case with complete necropsy.

Authors:  T BISLAND
Journal:  Am J Ophthalmol       Date:  1951-06       Impact factor: 5.258

2.  Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype.

Authors:  J F Rizzo; E L Berson; S Lessell
Journal:  Ophthalmology       Date:  1986-11       Impact factor: 12.079

3.  Histopathology of mitochondrial cytopathy and the Laurence-Moon-Biedl syndrome.

Authors:  P Runge; D Calver; J Marshall; D Taylor
Journal:  Br J Ophthalmol       Date:  1986-10       Impact factor: 4.638

4.  Pathology of Laurence-Moon-Bardet-Biedl syndrome.

Authors:  T G McLoughlin; D R Shanklin
Journal:  J Pathol Bacteriol       Date:  1967-01

5.  Laurence-Moon-Bardet-Biedl syndrome with Stargardt's juvenile macular degeneration. Clinical and pathological study.

Authors:  B Stănescu; F Nereanţu
Journal:  Ophthalmologica       Date:  1971       Impact factor: 3.250

6.  Three-dimensional structure of human retinal vessels studied by vascular casting.

Authors:  T Bek; P K Jensen
Journal:  Acta Ophthalmol (Copenh)       Date:  1993-08

7.  Bardet-Biedl syndrome and related disorders.

Authors:  A P Schachat; I H Maumenee
Journal:  Arch Ophthalmol       Date:  1982-02

8.  Laurence-Moon-Bardet-Biedl syndrome: electrophysical and psychophysical findings.

Authors:  O Katsumi; T Tanino; T Hirose; E W Larson; C J Skladzien
Journal:  Jpn J Ophthalmol       Date:  1985       Impact factor: 2.447

9.  Prevalence of retinitis pigmentosa and allied disorders in Denmark. II. Systemic involvement and age at onset.

Authors:  M Haim
Journal:  Acta Ophthalmol (Copenh)       Date:  1992-08

10.  Ocular and systemic manifestations of the Bardet-Biedl syndrome.

Authors:  R V Campo; T M Aaberg
Journal:  Am J Ophthalmol       Date:  1982-12       Impact factor: 5.258

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  4 in total

1.  An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosis.

Authors:  S Heegaard; T Rosenberg; M Preising; J U Prause; T Bek
Journal:  Br J Ophthalmol       Date:  2003-08       Impact factor: 4.638

2.  Genome-wide suppressor screen identifies USP35/USP38 as therapeutic candidates for ciliopathies.

Authors:  I-Chun Tsai; Kevin A Adams; Joyce A Tzeng; Omar Shennib; Perciliz L Tan; Nicholas Katsanis
Journal:  JCI Insight       Date:  2019-11-14

Review 3.  Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management.

Authors:  Sathya Priya; Sheela Nampoothiri; Parveen Sen; S Sripriya
Journal:  Indian J Ophthalmol       Date:  2016-09       Impact factor: 1.848

4.  Deletion in the Bardet-Biedl Syndrome Gene TTC8 Results in a Syndromic Retinal Degeneration in Dogs.

Authors:  Suvi Mäkeläinen; Minas Hellsand; Anna Darlene van der Heiden; Elina Andersson; Elina Thorsson; Bodil S Holst; Jens Häggström; Ingrid Ljungvall; Cathryn Mellersh; Finn Hallböök; Göran Andersson; Björn Ekesten; Tomas F Bergström
Journal:  Genes (Basel)       Date:  2020-09-18       Impact factor: 4.096

  4 in total

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