Article PDF
References
Small RG . Coats' disease and muscular dystrophy. Trans Am Acad Ophthalmol Otol 1968;72:225–31.
Coats G . Forms of retinal disease with massive exudation. R Lond Ophthalmic Hosp Rep 1908;17:440–525.
Gardner-Medwin D . New questions about the muscular dystrophies. Ann Rheum Dis 1995;54:536–8.
Uday R, et al. Long-term follow-up of facioscapulohumeral muscular dystrophy and Coats' disease. Am J Ophthalmol 1990;110:568–9.
Dickey JB, et al. Retinal telangiectasis in scapuloperoneal muscular dystrophy. Am J Ophthalmol 1991;112:348–9.
Yanoff M, Duke JS . Ophthalmology. St Louis: CV Mosby, 1999;8:23–0.4.
Black GC, Perveen R, et al. Coats' disease of the retina (unilateral telangiectasias) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis. Hum Mol Genet 1999;8:2031–5.
Meitinger T, Meindl A, et al. Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure. Nature Genet 1993;5:376–80.
Schroeder B, Hesse L, et al. Histopathological and immunohistochemical findings associated with a null mutation in the Norrie disease gene. Ophthalmic Genet 1997;18:71–7.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Bobart, A., Brosnahan, D. Coats' disease and Duchenne muscular dystrophy. Eye 15, 563–564 (2001). https://doi.org/10.1038/eye.2001.183
Issue Date:
DOI: https://doi.org/10.1038/eye.2001.183