Literature DB >> 2818284

Simple microphthalmos.

A H Weiss1, B G Kousseff, E A Ross, J Longbottom.   

Abstract

Simple microphthalmos was diagnosed in 22 patients on the basis of a normal-appearing eye and a total axial length at least 2 SDs below the mean for age. Anterior segment length was normal in most patients while posterior segment length was at least 2 SDs below the mean in all patients, indicating that disproportionate reduction in posterior segment length accounted for the microphthalmos. The normal values for total axial length, anterior segment length, and posterior segment length were determined from the analysis of axial length measurements obtained from age-similar controls. Ten patients had isolated microphthalmos. One of them was diagnosed as having nanophthalmos on the basis of microcornea, total axial length less than 18 mm, and absence of systemic disease. Twelve patients had associated systemic disorders, such as fetal alcohol syndrome, myotonic dystrophy, and achondroplasia, which implicated decreased size of the optic cup, altered vitreous proteoglycans, low intraocular pressure, and abnormal release of growth factors in the pathogenesis of microphthalmos.

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Year:  1989        PMID: 2818284     DOI: 10.1001/archopht.1989.01070020703032

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  27 in total

1.  Bony orbital maldevelopment after enucleation.

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2.  Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.

Authors:  M I Othman; S A Sullivan; G L Skuta; D A Cockrell; H M Stringham; C A Downs; A Fornés; A Mick; M Boehnke; D Vollrath; J E Richards
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3.  The nanophthalmic macula.

Authors:  J C Serrano; P R Hodgkins; D S Taylor; G A Gole; A Kriss
Journal:  Br J Ophthalmol       Date:  1998-03       Impact factor: 4.638

Review 4.  Genetic Advances in Microphthalmia.

Authors:  Julie Plaisancie; Patrick Calvas; Nicolas Chassaing
Journal:  J Pediatr Genet       Date:  2016-09-16

Review 5.  Classification of microphthalmos and coloboma.

Authors:  M Warburg
Journal:  J Med Genet       Date:  1993-08       Impact factor: 6.318

6.  High-hyperopia database, part I: clinical characterisation including morphometric (biometric) differentiation of posterior microphthalmos from nanophthalmos.

Authors:  N Relhan; S Jalali; N Pehre; H L Rao; U Manusani; L Bodduluri
Journal:  Eye (Lond)       Date:  2015-10-23       Impact factor: 3.775

7.  Unilateral high myopia: optical components, associated factors, and visual outcomes.

Authors:  A H Weiss
Journal:  Br J Ophthalmol       Date:  2003-08       Impact factor: 4.638

8.  Localization of a novel gene for congenital nonsyndromic simple microphthalmia to chromosome 2q11-14.

Authors:  Hui Li; Jia-Xin Wang; Cheng-Ye Wang; Ping Yu; Qiang Zhou; Yong-Gang Chen; Lu-Hang Zhao; Ya-Ping Zhang
Journal:  Hum Genet       Date:  2007-10-09       Impact factor: 4.132

9.  Aetiology of severe visual impairment and blindness in microphthalmos.

Authors:  M J Elder
Journal:  Br J Ophthalmol       Date:  1994-05       Impact factor: 4.638

10.  A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma.

Authors:  M A Reddy; P J Francis; V Berry; K Bradshaw; R J Patel; E R Maher; R Kumar; S S Bhattacharya; A T Moore
Journal:  Br J Ophthalmol       Date:  2003-02       Impact factor: 4.638

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