References
- Kohn R. Congenital anomalies of the eyelids and socket. In: Kohn R. Textbook of Ophthalmic Plastic and Reconstructive Surgery. Lea & Febiger, 1988;61–62.
- Kohn R. Congenital anomalies of the eyelids and socket. In: Hornblass A (editor). Oculoplastic, Orbital and Reconstructive Surgery. Baltimore: Williams & Wilkins, 1988;1o7-1o9.
- Zlotogora J, Sagi M, Cohen T. The Blepharophimosis, ptosis, and epicanthus inversus syndrome: delineation of two types. Am J Hum Genet. 1983;35:1020–1027.
- De Baere E, Dixon MJ, Small KW, et al. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation. HumMolec Genet. 2001;10(5): 1591–160o.
- De Baere E, Fukushima Y, Small K, et al. Identification of BPESCr, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES. Genomics. 2000:68: 296–304.
- Dollfus H, Kumaramanickavel Biswas P, et al. Identification of a new TWIST mutation (7p21) with variable eyelid manifestations supports locus homogeneity of BPES at 3923. J Med Genet. 2001; 58:470–471.
- Bell R, Murday VA, Patton MA, Jeffery S. Two families with blepharophimosis/ptosis/epicanthus inversus syndrome have mutations in the putative forkhead transcription factor FOXL2. Genet Test. 2001;5(4):335–338.
- Kosaki K, Ogata T, Kosaki R, Sato S, Matsuo N. A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid. Ophthalmic Genet. 2002;23(I):43–47.
- De Baere E, Beysen D, Oley C, et al. FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation. Am J Hum Genet. 2003; 72:478–487.
- Haase W Refraction in childhood as a risk factor for the development of amblyopia and/or strabismus. Recording a round table discussion at the 89th Congress of the German Society of Ophthalmology 25 September 1991 in Leipzig. Klin Monatsbl Augenheilkd. 1994;204(0:48–54.
- Gusek-Schneider G-C. Congenital ptosis: amblyogenic refractive errors, amblyopia, manifest strabismus and stereopsis related to the types of ptosis. Data on 77 patients and review of literature. Klin Monatsbl Augenheilkd. 2002;219: 340–348.
- Beaconsfield M, Walker J, Collin JR0. Visual development in the blepharophimosis syndrome. Br J Ophthalmol. 1991;75:746–748.
- Dray JP, Leibovitch I. Congenital ptosis and amblyopia: a retrospective study of 130 cases. J Pediatr Ophthalmol Strabismus. 2002;39(4):222–225.
- Ohlsson J, Villarrea G, Sjöström A, Abrahamsson M, Sjostrand J. Visual acuity, residual amblyopia and ocular pathology in a screened population of 12–13 year-old children in Sweden. Acta Ophthalmol Scand. 2001;79: 589–595.
- Sjostrand J, Abrahamsson M. Can we identify risk groups for the development of amblyopia and strabismus? Klin Monatsbl Augenheilkd. 1996;208(0:23–26.
- Von Noorden GK. Binocular Vision and Ocular Motility: Theory and Management of Strabismus. 5th ed. Missouri: Mosby, 1996;216.
- Brown SA, Weih LM, Fu CL, et al. Prevalence of amblyopia and associated refractive errors in an adult population in Victoria, Australia. Ophthalmic Epidemiol. 2000;7(4):249–258.
- Atkinson J, Braddick 0, Robier B, et al. Two infant vision screening programmes: prediction and prevention of strabismus and amblyopia from photo- and videorefractive screening. Eye. 1996;m\(Pt 2):189–I98.
- Abrahamsson M, Fabian G, Andersson AK, Sjostrand J. A longitudinal study of a population based sample of astigmatic children. I. Refraction and amblyopia. Acta Ophthalmol (Copenh). 1990;68(4): 428–434.
- Abrahamsson M, Fabian G, Sjostrand J. Changes in astigmatism between the ages of i and 4 years: a longitudinal study. Br J Ophthalmol. 1988;72(2):145–149.