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[Simultaneous corneal transplantation in mucopolysaccharidosis].

作者信息

Orgül S, Daicker B, Kain H L

机构信息

Universitäts-Augenklinik Basel.

出版信息

Klin Monbl Augenheilkd. 1991 May;198(5):430-2. doi: 10.1055/s-2008-1046001.

DOI:10.1055/s-2008-1046001
PMID:1909396
Abstract

We report the case of a 14 year old girl who obtained simultaneous penetrating keratoplasty for corneal opacity with functional loss as a consequence of a mucopolysaccharidosis typ Hurler/Scheie. Postoperatively, the host cornea displayed partial clearing. We discuss mechanisms possibly involved.

摘要

相似文献

1
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Klin Monbl Augenheilkd. 1991 May;198(5):430-2. doi: 10.1055/s-2008-1046001.
2
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[Mucopolysaccharidosis type I, Hurler-Scheie phenotype with ocular involvement. Clinical and ultrastructural study].[I型黏多糖贮积症,伴有眼部受累的Hurler-Scheie表型。临床和超微结构研究]
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Corneal topometric, aberrometric and biomechanical parameters in mucopolysaccharidosis patients.黏多糖贮积症患者的角膜地形学、像差和生物力学参数。
PLoS One. 2019 Jun 27;14(6):e0218108. doi: 10.1371/journal.pone.0218108. eCollection 2019.
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Does enzyme replacement therapy influence the ocular changes in type VI mucopolysaccharidosis?酶替代疗法会影响 VI 型黏多糖贮积症的眼部变化吗?
Graefes Arch Clin Exp Ophthalmol. 2009 Jul;247(7):975-80. doi: 10.1007/s00417-008-1030-1. Epub 2009 Jan 22.