Literature DB >> 6943836

Congenital myopia and retinal detachment.

J D Scott.   

Abstract

Retinal detachment is unusual in children and is often associated with other serious ocular abnormalities. In more than 25 children varying in age from 3 to 16 years in whom the common ocular complication was congenital myopia, associated features included facial abnormalities and other changes often associated with familial and inherited conditions. A very high incidence of giant retinal breaks was found and these were associated with considerable difficulty in treatment.

Entities:  

Mesh:

Year:  1980        PMID: 6943836

Source DB:  PubMed          Journal:  Trans Ophthalmol Soc U K        ISSN: 0078-5334


  4 in total

1.  Vitreous phenotype: genotype correlation in Stickler syndrome.

Authors:  David McLeod; Graeme C M Black; Paul N Bishop
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2002-01       Impact factor: 3.117

2.  The pseudo-posterior limiting layer syndrome: a vitreoretinal heredodegeneration with autosomal dominant transmission. Graefe's Arch Clin Exp Ophthalmol (1994) 232:16-24.

Authors:  M P Snead; D K Newmann; A Poulson; J D Scott
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1995-12       Impact factor: 3.117

3.  A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene.

Authors:  Guy Van Camp; Rikkert L Snoeckx; Nele Hilgert; Jenneke van den Ende; Hisakumi Fukuoka; Michio Wagatsuma; Hiroaki Suzuki; R M Erica Smets; Filip Vanhoenacker; Frank Declau; Paul Van de Heyning; Shin-ichi Usami
Journal:  Am J Hum Genet       Date:  2006-06-26       Impact factor: 11.025

4.  Retinal detachment in identical twins with Stickler syndrome type 1.

Authors:  Y Watanabe; M Ueda; E Adachi-Usami
Journal:  Br J Ophthalmol       Date:  1996-11       Impact factor: 4.638

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.