Literature DB >> 2920912

Fine structural defects in a case of congenital microcoria.

J M Butler1, G Raviola, C D Miller, A I Friedmann.   

Abstract

A case of congenital miosis associated with myopia and cataract is described. Tissue obtained at iridectomy was examined with the electron microscope and compared with a specimen of normal iris. The miotic iris was found to be hypoplastic and to display differences in the cellular density of the stroma. The contractile processes of the dilator myoepithelium were conspicuously absent from the underlying stroma, and the existing myofibrils were much disarranged.

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Year:  1989        PMID: 2920912     DOI: 10.1007/BF02169832

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  5 in total

1.  CONGENITAL MIOSIS OR PINHOLE PUPILS OWING TO DEVELOPMENTAL FAULTS OF THE DILATATOR MUSCLE.

Authors:  S Holth; O Berner
Journal:  Br J Ophthalmol       Date:  1923-09       Impact factor: 4.638

2.  A CASE OF CONGENITAL MIOSIS.

Authors:  T H Cresswell
Journal:  Br J Ophthalmol       Date:  1924-06       Impact factor: 4.638

Review 3.  The structural basis of the blood-ocular barriers.

Authors:  G Raviola
Journal:  Exp Eye Res       Date:  1977       Impact factor: 3.467

4.  The Marfan syndrome. A histopathologic study of ocular findings.

Authors:  M S Ramsey; B S Fine; J A Shields; M Yanoff
Journal:  Am J Ophthalmol       Date:  1973-07       Impact factor: 5.258

5.  The homogeneous structure of blood vessels in the vascular tree of Macaca mulatta iris.

Authors:  T F Freddo; G Raviola
Journal:  Invest Ophthalmol Vis Sci       Date:  1982-03       Impact factor: 4.799

  5 in total
  5 in total

1.  Genotypic and phenotypic heterogeneity in familial microcoria.

Authors:  F D Bremner; H Houlden; S E Smith
Journal:  Br J Ophthalmol       Date:  2004-04       Impact factor: 4.638

2.  Megalocornea. Clinical and genetic aspects.

Authors:  F M Meire
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

3.  Submicroscopic deletions at 13q32.1 cause congenital microcoria.

Authors:  Lucas Fares-Taie; Sylvie Gerber; Akihiko Tawara; Arturo Ramirez-Miranda; Jean-Yves Douet; Hannah Verdin; Antoine Guilloux; Juan C Zenteno; Hiroyuki Kondo; Hugo Moisset; Bruno Passet; Ken Yamamoto; Masaru Iwai; Toshihiro Tanaka; Yusuke Nakamura; Wataru Kimura; Christine Bole-Feysot; Marthe Vilotte; Sylvie Odent; Jean-Luc Vilotte; Arnold Munnich; Alain Regnier; Nicolas Chassaing; Elfride De Baere; Isabelle Raymond-Letron; Josseline Kaplan; Patrick Calvas; Olivier Roche; Jean-Michel Rozet
Journal:  Am J Hum Genet       Date:  2015-03-12       Impact factor: 11.025

Review 4.  Congenital Microcoria: Clinical Features and Molecular Genetics.

Authors:  Clémentine Angée; Brigitte Nedelec; Elisa Erjavec; Jean-Michel Rozet; Lucas Fares Taie
Journal:  Genes (Basel)       Date:  2021-04-22       Impact factor: 4.096

5.  Ultrabiomicroscopic-histopathologic correlations in individuals with autosomal dominant congenital microcoria: three-generation family report.

Authors:  Arturo Ramirez-Miranda; Juan M Paulin-Huerta; Eduardo Chavez-Mondragón; Gilberto Islas-de la Vega; Abelardo Rodriguez-Reyes
Journal:  Case Rep Ophthalmol       Date:  2011-05-13
  5 in total

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