Literature DB >> 4028500

Autosomal dominant cataract and microcornea associated with myopia in a Sicilian family.

F Mollica, S Li Volti, S Tomarchio, A Gangi, V Risiglione, G Gorgone.   

Abstract

A Sicilian family is reported in which 36 individuals, in 5 successive generations, were affected with congenital cataracts, microcornea and myopia with an autosomal pattern of inheritance.

Entities:  

Mesh：

Year:  1985        PMID： 4028500     DOI： 10.1111/j.1399-0004.1985.tb01216.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


  4 in total

1.  Bilateral congenital dentiform cataract and extreme microcornea in eyes with uveal colobomas and persistent hyperplastic primary vitreous.

Authors:  B Seitz; G O Naumann
Journal:  Br J Ophthalmol       Date:  1996-04       Impact factor: 4.638

2.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

3.  Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family.

Authors:  R V Jamieson; F Munier; A Balmer; N Farrar; R Perveen; G C M Black
Journal:  Br J Ophthalmol       Date:  2003-04       Impact factor: 4.638

4.  Microcornea associated with myopia.

Authors:  Zoltán Sohajda; Dóra Holló; András Berta; László Módis
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2006-02-23       Impact factor: 3.117
  4 in total

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