Literature DB >> 2019954

Heterotopic ciliary epithelial differentiation in a patient with trisomy 13.

J J Michon1, J M Borges, M O Tso.   

Abstract

A premature infant was born with congenital anomalies suggestive of trisomy 13, confirmed by karyotype analysis. Pathologic examination of the eyes revealed typical features of trisomy 13, including microphthalmos, extensive colobomata, and retinal dysplasia. A heterotopic ciliary body had also developed in the posterior segment of the left eye in the region of the posterior coloboma. The development of a well-formed ciliary body in the posterior segment of the eye questions the hypothesis that physical contact between the lens primordium and neuroepithelium is required for ciliary body development.

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Year:  1991        PMID: 2019954

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  2 in total

1.  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

2.  Unilateral sporadic retinal dysplasia: results of histopathologic, immunohistochemical, chromosomal, genetic, and VEGF-A analyses.

Authors:  Frederick A Jakobiec; Fouad R Zakka; Robert D'Amato; Margaret M Deangelis; David S Walton; Rajesh C Rao
Journal:  J AAPOS       Date:  2011-12       Impact factor: 1.220

  2 in total

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