Literature DB >> 1776417

Congenital ectopia lentis and secondary buphthalmos likely occurring as an autosomal recessive trait.

K Bjerrum1, S V Kessing.   

Abstract

A family from Turkey with congenital ectopia lentis, likely occurring as an autosomal recessive trait, is presented. No systemic disorders such as homocysteinuria, Marfan's or Weill-Marchesani's syndromes were found in any of the patients. However, all patients except one were less than 2 years old when first examined so that lens luxation must have happened very early in life. Besides almost total lack of zonular threads the patients presented anomalies of ocular dimensions with increased corneal diameters and axial lengths, and in several cases glaucomatous distension of the optic discs could also be found. A possible explanation for these buphthalmic changes and their relation to lens luxation taking place very early in life is proposed. The importance of early diagnosis and treatment is discussed.

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Year:  1991        PMID: 1776417     DOI: 10.1111/j.1755-3768.1991.tb04851.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


  2 in total

1.  A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis.

Authors:  Dina Ahram; T Shawn Sato; Abdulghani Kohilan; Marwan Tayeh; Shan Chen; Suzanne Leal; Mahmoud Al-Salem; Hatem El-Shanti
Journal:  Am J Hum Genet       Date:  2009-02-05       Impact factor: 11.025

2.  Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations.

Authors:  Arif O Khan; Mohammed A Aldahmesh; Fowzan S Alkuraya
Journal:  Mol Vis       Date:  2011-10-04       Impact factor: 2.367

  2 in total

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