April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Corneal Opacities in Trisomy 8 Mosaic Syndrome : Clinical, Histologic and Genetic Features
Author Affiliations & Notes
  • M.-C. Gaillard
    Ophthalmology, Jules Gonin Eye Hospital, Lausanne, Switzerland
    Medical genetics, Centre hospitalier vaudois, Lausanne, Switzerland
  • F. Majo
    Ophthalmology, Jules Gonin Eye Hospital, Lausanne, Switzerland
  • A. Moulin
    Ophthalmology, Jules Gonin Eye Hospital, Lausanne, Switzerland
  • S. Uffer
    Ophthalmology, Jules Gonin Eye Hospital, Lausanne, Switzerland
  • D. Marinet
    Medical Genetics, Centre Hospitalier Vaudois, Lausanne, Switzerland
  • F. Niel Bütschi
    Medical Genetics, Centre Hospitalier Vaudois, Lausanne, Switzerland
  • F. L. Munier
    Ophthalmology, Jules Gonin Eye Hospital, Lausanne, Switzerland
  • Footnotes
    Commercial Relationships  M.-C. Gaillard, None; F. Majo, None; A. Moulin, None; S. Uffer, None; D. Marinet, None; F. Niel Bütschi, None; F.L. Munier, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 4654. doi:
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      M.-C. Gaillard, F. Majo, A. Moulin, S. Uffer, D. Marinet, F. Niel Bütschi, F. L. Munier; Corneal Opacities in Trisomy 8 Mosaic Syndrome : Clinical, Histologic and Genetic Features. Invest. Ophthalmol. Vis. Sci. 2010;51(13):4654.

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Abstract

Purpose: : To describe the clinical, histologic and genetic findings of corneal opacities in the trisomy 8 mosaic syndrome.

Methods: : 3 children aged 8 years (Patients A), 6 years (Patients B) and 1 month (Patients C) respectively, were referred with corneal opacities for ophthalmologic evaluation. The 2 older patients had been previously diagnosed with trisomy 8 mosaicism, while the third was diagnosed after the ocular examination. Automated lamellar keratoplasty (ALTK) was performed on the most amblyopic eye. Histopathologic analysis with immunohistochemical markers and cytogenetic studies by FISH using haploid probes for chromosome 8 and chromosome 16 (control) were performed on the excised corneal lesion.

Results: : All patients presented vascularized corneal opacities involving the superficial stroma, and amblyopia with a bilateral involvement in two of them (Patients A and B). Post-operative follow-up (range 6-20 months) was satisfactory, with the graft remaining clear and improved visual acuity, allowing iso-acuity and stereoscopy in the one month old child (Patients C).The clinically observed corneal opacities corresponded histopathologically to the replacement of the normal anterior corneal stroma by a choristomatous loose richly vascularized connective tissue containing mucopolysacharides. Bowman's membrane was absent. There were no adnexal structures. The overlaying epithelium expressed keratin 3 in all three cases. Keratin 19 was found in the suprabasal epithelial cells in one case but was absent in the other cases. There were no expression of keratin 7 and 1 as well as MUC5AC in the epithelial cells.FISH analysis from 100 interphase cells of the affected tissue and normal conjontival probe revealed normal diploid cells.

Conclusions: : In this series, the corneal opacities associated with trisomy 8 mosaic syndrome share a common clinical, histopathological and genetic features. ALTK should be considered at diagnosis to prevent amblyopia in these children.

Keywords: cornea: epithelium • immunohistochemistry • fluorescent in situ hybridization 
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