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The Ocular Manifestation of Turner Syndrome

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Optic Disorders and Visual Field

Part of the book series: Advances in Visual Science and Eye Diseases ((AVSED,volume 2))

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Abstract

Turner syndrome is a sex chromosome disease caused by abnormalities in chromosome number or structure. Ocular dysplasia can be found in such patients [1, 2]. The visual field change in a Turner syndrome case is introduced in this section, and karyotypic abnormalities and chimerism are also analyzed.

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References

  1. Denniston AK, Butler L. Ophthalmic features of Turner’s syndrome. Eye. 2004;18(7):680–4.

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  2. Wikiera B, Mulak M, Koltowska-Haggstrom M, et al. The presence of eye defects in patients with Turner syndrome is irrespective of their karyotype. Clin Endocrinol. 2015;83(6):842–8.

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  4. Birkebaek NH, Crüger D, Hansen J, et al. Fertility and pregnancy outcome in Danish women with Turner syndrome. Clin Genet. 2002;61(1):35–9.

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© 2019 Springer Nature Singapore Pte Ltd. & People's Medical Publishing House, PR of China

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Fan, N., Liu, X., Wang, J. (2019). The Ocular Manifestation of Turner Syndrome. In: Wang, N., Liu, X., Fan, N. (eds) Optic Disorders and Visual Field. Advances in Visual Science and Eye Diseases, vol 2. Springer, Singapore. https://doi.org/10.1007/978-981-13-2502-1_21

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  • DOI: https://doi.org/10.1007/978-981-13-2502-1_21

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  • Publisher Name: Springer, Singapore

  • Print ISBN: 978-981-13-2501-4

  • Online ISBN: 978-981-13-2502-1

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