Rare diseases of sigth

Authors

DOI:

https://doi.org/10.3989/arbor.2018.789n3004

Keywords:

Inherited retinal dystrophies, optic nerve, corneal dystrophies, disorders of eye development

Abstract


A large number of rare pathologies affect the eye or sight. A possible classification of these is according to the tissue that is affected. We can, therefore, define three main types of rare ocular disorders: 1) neuro-ocular pathologies, which basically affects the retina and optic nerve, 2) corneal dystrophies and 3) pathologies caused by deficiencies in the development of the eyeball or any of its parts. In all of them there is a clear Mendelian genetic basis and, currently, there is almost no treatment for any of them. The aim of this article is to provide a review of this set of pathologies.

Downloads

Download data is not yet available.

References

Ayuso, C. y Millán, J. M. (2010). Retinitis pigmentosa and allied conditions today: a paradigm of translational research. Genome Medicine, 2 (5), 34. https://doi.org/10.1186/gm155 PMid:20519033 PMCid:PMC2887078

Cepko, C. L. (2005). Effect of gene expression on cone survival in retinitis pigmentosa. Retina, 25 (8), pp. S21-S24. https://doi.org/10.1097/00006982-200512001-00008

Fuhrmann, S. (2010). Eye morphogenesis and patterning of the optic vesicle. Current Topics in Developmental Biology, 93, pp. 61-84. https://doi.org/10.1016/B978-0-12-385044-7.00003-5 PMid:20959163 PMCid:PMC2958684

Hamel, C. P. (2007). Cone rod dystrophies. Orphanet Journal of Rare Diseases, 2 (1), 7. https://doi.org/10.1186/1750-1172-2-7 PMid:17270046 PMCid:PMC1808442

Khanna, H. y Baehr, W. (2012). Retina ciliopathies: from genes to mechanisms and treatment. Vision Research, 75, p. 1. https://doi.org/10.1016/j.visres.2012.11.007 PMid:23206575

Klintworth, G. K. (2009). Corneal dystrophies. Orphanet Journal of Rare Diseases, 4 (1), 7. https://doi.org/10.1186/1750-1172-4-7 PMid:19236704 PMCid:PMC2695576

Lodha, N., Loucks, C. M., Beaulieu, C., Parboosingh, J. S. y Bech-Hansen, N. T. (2012). Congenital stationary night blindness: mutation update and clinical variability. En LaVail, M., Ash, J., Anderson R., Hollyfield, J. y Grimm, C. (eds.). Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology, pp. 371-379. https://doi.org/10.1007/978-1-4614-0631-0_48

Ramamurthy, V. y Cayouette, M. (2009). Development and disease of the photoreceptor cilium. Clinical Genetics, 76 (2), pp. 137-145. https://doi.org/10.1111/j.1399-0004.2009.01240.x

Roosing, S., Thiadens, A. A., Hoyng, C. B., Klaver, C. C., Hollander, A. I. den y Cremers, F. P. (2014). Causes and consequences of inherited cone disorders. Progress in Retinal and Eye Research, 42, pp. 1-26. https://doi.org/10.1016/j.preteyeres.2014.05.001 PMid:24857951

You, Y., Gupta, V. K., Li, J. C., Klistorner, A. y Graham, S. L. (2013). Optic neuropathies: characteristic features and mechanisms of retinal ganglion cell loss. Reviews in the Neurosciences, 24 (3), pp. 301-321. https://doi.org/10.1515/revneuro-2013-0003

Published

2018-09-30

How to Cite

Millán Salvador, J. M. (2018). Rare diseases of sigth. Arbor, 194(789), a462. https://doi.org/10.3989/arbor.2018.789n3004

Issue

Section

Articles