Literature DB >> 17725279

[An analysis of the fundus changes in families with high myopia].

Agata Frajdenberg1, Krystyna Pecold, Monika Podfigurna-Musielak, Małgorzata Rydzanicz, Małgorzata Mrugacz, Suzanne M Leal, Bassem A Bejjani, Marzena Gajecka.   

Abstract

PURPOSE: Of this study is to present fundus changes in members of families with high myopia.
MATERIAL AND METHODS: Detailed clinical examination of the enrolled subjects have been performed in the high myopia families. Both affected (presented with high myopia) and unaffected individuals (without high myopia) are given an ophthalmologic examination: best-corrected visual acuity testing, intraocular pressure examination, fundoscopy, axial length determination (using ultrasonography), refractometry.
RESULTS: In the 19 high myopia families, 152 individuals were carefully examined. In 11 individuals retinal detachment have been observed. Additionally, myopic degeneration of the central retina (15 cases), degeneration of the peripherial retina (20 subjects), AMD (4 subjects), hypertrophy of the RPE (2 subjects), CNV (1 case), striae medullares (1 case) and macular foramen (1 case), have been identified.
CONCLUSIONS: In the affected individuals (presented with high myopia) changes of the eye fundus and retinal detachment were more frequently observed comparing to unaffected members of the families without high myopia. In unaffected individuals genetic factor seems to play insignificant role in apperance of fundus. Changes within central retina in the high myopia individuals may conduce to severe visual impairment.

Entities:  

Mesh:

Year:  2007        PMID: 17725279      PMCID: PMC6190802     

Source DB:  PubMed          Journal:  Klin Oczna        ISSN: 0023-2157


  13 in total

1.  A genome wide scan for familial high myopia suggests a novel locus on chromosome 7q36.

Authors:  L Naiglin; C Gazagne; F Dallongeville; C Thalamas; A Idder; O Rascol; F Malecaze; P Calvas
Journal:  J Med Genet       Date:  2002-02       Impact factor: 6.318

2.  Retinal detachment associated with a macular hole in severely myopic eyes.

Authors:  J Akiba; S Konno; A Yoshida
Journal:  Am J Ophthalmol       Date:  1999-11       Impact factor: 5.258

Review 3.  [Epidemiology of myopia].

Authors:  A Pechmann; D Czepita
Journal:  Klin Oczna       Date:  2000

4.  A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612.

Authors:  Qingjiong Zhang; Xiangming Guo; Xueshan Xiao; Xiaoyun Jia; Shiqiang Li; J Fielding Hejtmancik
Journal:  Mol Vis       Date:  2005-07-22       Impact factor: 2.367

5.  Epidemiologic study of ocular refraction among schoolchildren in Taiwan in 1995.

Authors:  L L Lin; Y F Shih; C B Tsai; C J Chen; L A Lee; P T Hung; P K Hou
Journal:  Optom Vis Sci       Date:  1999-05       Impact factor: 1.973

6.  The influence of refractive error and lattice degeneration on the incidence of retinal detachment.

Authors:  T C Burton
Journal:  Trans Am Ophthalmol Soc       Date:  1989

7.  [The causes of childhood blindness and visual impairment in Poland].

Authors:  M Seroczyńska; M E Prost; J Medruń; E Łukasiak; E Oleksiak
Journal:  Klin Oczna       Date:  2001

8.  New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.

Authors:  Prasuna Paluru; Shawn M Ronan; Elise Heon; Marcella Devoto; Scott C Wildenberg; Genaro Scavello; Ann Holleschau; Outi Mäkitie; William G Cole; Richard A King; Terri L Young
Journal:  Invest Ophthalmol Vis Sci       Date:  2003-05       Impact factor: 4.799

9.  The relationship between glaucoma and myopia: the Blue Mountains Eye Study.

Authors:  P Mitchell; F Hourihan; J Sandbach; J J Wang
Journal:  Ophthalmology       Date:  1999-10       Impact factor: 12.079

10.  Evidence that a locus for familial high myopia maps to chromosome 18p.

Authors:  T L Young; S M Ronan; L A Drahozal; S C Wildenberg; A B Alvear; W S Oetting; L D Atwood; D J Wilkin; R A King
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

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