Literature DB >> 14644246

A case of Kniest dysplasia with retinal detachment and the mutation analysis.

Toshiyuki Yokoyama1, Satoru Nakatani, Akira Murakami.   

Abstract

PURPOSE: To report a case of Kniest dysplasia with retinal detachment associated with a novel type II collagen gene (COL2A1) mutation.
DESIGN: Interventional case report.
METHODS: DNA was isolated from peripheral lymphocytes, and mutational analysis was carried out using polymerase chain reaction and direct sequencing.
RESULTS: A 14-year-old Japanese boy was diagnosed with Kniest dysplasia, and ophthalmic examination revealed a retinal detachment in the right eye. He was successfully treated by vitrectomy and silicon oil injection, and his visual acuity improved from 0.01 to 0.22. DNA analysis of COL2A1 revealed a single base-pair substitution at position +5 of intron 20.
CONCLUSION: Vitrectomy and silicon oil injection were effective in reattaching the retinal detachment in a Kniest dysplasia patient. The genetic alteration found in this patient suggested that this prevented the normal splicing of COL2A1, resulting in an abnormal type II collagen product.

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Year:  2003        PMID: 14644246     DOI: 10.1016/s0002-9394(03)00713-x

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  1 in total

1.  Ophthalmic and molecular genetic findings in Kniest dysplasia.

Authors:  P I Sergouniotis; G S Fincham; A M McNinch; C Spickett; A V Poulson; A J Richards; M P Snead
Journal:  Eye (Lond)       Date:  2015-01-16       Impact factor: 3.775

  1 in total

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