References
1. Shields JA, Shields CL. Review: Coats disease: the 2001 LuEsther T. Mertz lecture. Retina. 2002; 22:80–91.
2. Shields JA, Shields CL, Honavar S, Demirci H. Coats disease. Clinical variations and complications of Coats disease in 150 cases. The 2000 Sanford Gifford Memorial Lecture. Am J Ophthalmol. 2001; 31:561–71.
3. Shields JA, Shields CL, Honavar SG, et al. Classification and management of Coats disease. The 2000 Proctor Lecture. Am J Ophthalmol. 2001; 131:572–83.
4. Ma DJ, Choi J, Jang JW, et al. Bilateral Coats' disease: A case report. J Korean Ophthalmol Soc. 2011; 52:112–6.
1. Bass SJ, Sherman J, Giovinazzo V. Bilateral Coats’ response in a female patient leads to diagnosis of facioscapulohumeral muscular dystrophy. Optometry. 2011; 82:72–6.
2. Bindoff LA, Mjellem N, Sommerfelt K, et al. Severe fas-cioscapulohumeral muscular dystrophy presenting with Coats’ disease and mental retardation. Neuromuscul Disord. 2006; 16:559–63.
3. Gurwin EB, Fitzsimons RB, Sehmi KS, Bird AC. Retinal te-langiectasis in facioscapulohumeral muscular dystrophy with deafness. Arch Ophthalmol. 1985; 103:1695–700.
4. Shields CL, Zahler J, Falk N, et al. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child. Arch Ophthalmol. 2007; 125:840–2.
5. Taylor DA, Carroll JE, Smith ME, et al. Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome. Ann Neurol. 1982; 12:395–8.