Literature DB >> 2818283

Complex microphthalmos.

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

Abstract

Forty patients were diagnosed as having complex microphthalmos on the basis of a malformed globe with a total axial length measurement at least 2 SDs below the mean for age-similar controls. Three had anterior segment dysgenesis; 4, congenital lens abnormalities; 14, chorioretinal colobomas; 12, persistent hyperplastic primary vitreous; 4, retinal dysplasia; and 3, complex malformations due to ipsilateral facial malformations. Measurements of total axial length indicated that complex microphthalmos was congenital and that postnatal growth of the malformed eye was similar to that of normal eyes. In most patients the anterior segment length was normal, while in all patients the posterior segment length was at least 2 SDs below the mean. Corneal diameter correlated significantly with total axial length (r2 = .57) and decreased linearly as total axial length decreased. In most patients in whom measurements were obtained, the lens and corneal power were increased, thereby compensating for decreased total axial length. We propose that inadequate production of secondary vitreous is the cause of the microphthalmos, given that the posterior segment was disproportionately reduced in size and the secondary vitreous is its predominant component. Evidence that each of the various ocular malformations can influence the production of secondary vitreous is presented.

Entities:  

Mesh:

Year:  1989        PMID: 2818283     DOI: 10.1001/archopht.1989.01070020697031

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


  20 in total

1.  Clinical utility gene card for: Non-Syndromic Microphthalmia Including Next-Generation Sequencing-Based Approaches.

Authors:  Rose Richardson; Jane Sowden; Christina Gerth-Kahlert; Anthony T Moore; Mariya Moosajee
Journal:  Eur J Hum Genet       Date:  2017-01-18       Impact factor: 4.246

Review 2.  Genetic Advances in Microphthalmia.

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

Review 3.  Classification of microphthalmos and coloboma.

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

4.  Dominantly inherited unilateral retinal dysplasia.

Authors:  I C Lloyd; A Colley; A B Tullo; R Bonshek
Journal:  Br J Ophthalmol       Date:  1993-06       Impact factor: 4.638

5.  Cataract surgery in infants with microphthalmos.

Authors:  Shrikant Prasad; Jagat Ram; Jaspreet Sukhija; Surinder Singh Pandav; Parul Chawla Gupta
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-01-16       Impact factor: 3.117

6.  The familial contribution to non-syndromic ocular coloboma in south India.

Authors:  S J Hornby; L Dandona; R B Jones; H Stewart; C E Gilbert
Journal:  Br J Ophthalmol       Date:  2003-03       Impact factor: 4.638

7.  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

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

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

9.  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

10.  Clinical and genetic features of a dominantly-inherited microphthalmia pedigree from China.

Authors:  Changhong Yu; Zhengmao Hu; Jingzhi Li; Ting Liu; Kun Xia; Lixin Xie
Journal:  Mol Vis       Date:  2009-05-08       Impact factor: 2.367

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